{"id":6339,"date":"2025-03-30T21:57:41","date_gmt":"2025-03-30T19:57:41","guid":{"rendered":"https:\/\/genorama.com\/kkk\/"},"modified":"2026-04-06T15:12:49","modified_gmt":"2026-04-06T13:12:49","slug":"kkk","status":"publish","type":"page","link":"https:\/\/genorama.com\/et\/kkk\/","title":{"rendered":"KKK"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"6339\" class=\"elementor elementor-6339 elementor-3956\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-f700e31 elementor-section-full_width elementor-section-height-min-height elementor-section-height-default elementor-section-items-middle\" data-id=\"f700e31\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;,&quot;shape_divider_top&quot;:&quot;wave-brush&quot;,&quot;shape_divider_bottom&quot;:&quot;wave-brush&quot;}\">\n\t\t\t\t\t\t\t<div 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d=\"M15.6,13.2c0-0.1,4.3,0,6.7,0.5c2.4,0.5,5,1.9,5,2c0,0.1-2.7-0.8-5.1-1.4\tC19.9,13.7,15.7,13.3,15.6,13.2z\"\/>\n<\/svg>\t\t<\/div>\n\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-ca594b6\" data-id=\"ca594b6\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-7901108 elementor-widget elementor-widget-heading\" data-id=\"7901108\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-xxl\">Korduma Kippuvad K\u00fcsimused<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-5fe5621 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"5fe5621\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-1f30617\" data-id=\"1f30617\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-f2f84d3 elementor-widget elementor-widget-spacer\" data-id=\"f2f84d3\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-25c578e elementor-widget elementor-widget-heading\" data-id=\"25c578e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Kui te ei leia vastust oma k\u00fcsimusele allpool, v\u00f5tke meiega \u00fchendust.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f00fe53 elementor-widget elementor-widget-toggle\" data-id=\"f00fe53\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"toggle.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-toggle\">\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2511\" class=\"elementor-tab-title\" data-tab=\"1\" role=\"button\" aria-controls=\"elementor-tab-content-2511\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">K: Kuidas tellida ja registreerida oma testi?<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2511\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"1\" role=\"region\" aria-labelledby=\"elementor-tab-title-2511\"><p><span style=\"color: #333333;\"><strong>K: Kuidas tellida testi?<\/strong><\/span><\/p><p>Oma testi tellimiseks valige lihtsalt soovitud test veebilehe \u00fclaosas olevast poe men\u00fc\u00fcst, kasutage <a href=\"https:\/\/genorama.com\/et\/contact\/\">kontaktivormi<\/a> v\u00f5i saatke meile e-kiri aadressil \u201einfo@genorama.com\u201c. Lisateavet erinevate testide kohta saate lugeda, kui kl\u00f5psate kataloogist neile.<\/p><p><span style=\"color: #333333;\"><strong>K: Kuidas ma registreerin oma testi ja saan juurdep\u00e4\u00e4su tulemustele?<\/strong><\/span><\/p><p>Et tagada v\u00f5imalikult suur turvalisus ja konfidentsiaalsus, oleme v\u00e4lja t\u00f6\u00f6tanud spetsiaalse kliendiportaali. Protsessi algatamiseks registreerige oma test <a href=\"https:\/\/genorama.com\/et\/portaal\/\">siin<\/a> lingitud portaali kaudu. Testipaki sees leiate unikaalse koodi, mida vajate registreerimiseks.<\/p><p>P\u00e4rast registreerimist palume teil t\u00e4ita l\u00fchike k\u00fcsitlus. See v\u00f5imaldab meil koguda olulist teavet teie proovi p\u00f5hjalikuks anal\u00fc\u00fcsiks. Kui k\u00fcsitlus on esitatud, registreeritakse teie test ametlikult. Seej\u00e4rel saate oma proovi meile tagasi saata, j\u00e4rgides pakendile lisatud juhiseid.<\/p><p>Soovitame teil s\u00e4ilitada proovi tagastamiseks pakendikarbi. P\u00e4rast proovi laborisse tagasi j\u00f5udmist alustame kohe anal\u00fc\u00fcsiga. Kui anal\u00fc\u00fcs on l\u00f5petatud, laaditakse tulemused turvaliselt \u00fcles kliendiportaali. Saate oma tulemustele ligi ja neid alla laadida, kasutades registreerimisfaasis kehtestatud 2-tegurilist autentimist.<\/p><p>Pange t\u00e4hele, et privaatsuse ja turvalisuse huvides oleme kohustatud tulemused kliendiportaalist eemaldama p\u00e4rast teatud aja m\u00f6\u00f6dumist tulemuste allalaadimisest. Soovitame teil s\u00e4ilitada oma tulemuste koopia edaspidiseks kasutamiseks. Kui teil on mingeid probleeme v\u00f5i vajate t\u00e4iendavat abi, v\u00f5tke julgelt \u00fchendust meie klienditoega.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2512\" class=\"elementor-tab-title\" data-tab=\"2\" role=\"button\" aria-controls=\"elementor-tab-content-2512\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">K: Kuidas on minu andmed ja tulemused kaitstud?<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2512\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"2\" role=\"region\" aria-labelledby=\"elementor-tab-title-2512\"><p>Meie prioriteediks on teie andmete ja tulemuste turvalisus. Kahefaktorilise autentimise ja kr\u00fcpteeritud veebip\u00f5hise kasutajaportaali abil tagame, et ainult teie saate juurdep\u00e4\u00e4su oma geenitestide tulemustele. Regulaarsed turvaauditid ja andmekaitse-eeskirjade j\u00e4rgimine tugevdavad veelgi meie p\u00fchendumust teie andmete kaitsmisele.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2513\" class=\"elementor-tab-title\" data-tab=\"3\" role=\"button\" aria-controls=\"elementor-tab-content-2513\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">K: Kuidas proove \u00f5igesti v\u00f5tta?<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2513\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"3\" role=\"region\" aria-labelledby=\"elementor-tab-title-2513\"><h3>P\u00f5sekaape kogumispulga kasutusjuhend<\/h3>\n<p><p class=\"responsive-video-wrap clr\"><iframe title=\"P\u00f5sekaape kogumispulga kasutusjuhend | Genorama\" width=\"1200\" height=\"675\" src=\"https:\/\/www.youtube.com\/embed\/nAi6Lva0gCU?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" referrerpolicy=\"strict-origin-when-cross-origin\" allowfullscreen><\/iframe><\/p><\/p>\n<p>&nbsp;<\/p>\n<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2514\" class=\"elementor-tab-title\" data-tab=\"4\" role=\"button\" aria-controls=\"elementor-tab-content-2514\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">K: Mida peaksin silmas pidama, kui tellin sugulustesti?<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2514\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"4\" role=\"region\" aria-labelledby=\"elementor-tab-title-2514\"><p>Bioloogiliste sugulussuhete testimine v\u00f5imaldab lisaks isaduse kindlakstegemisele tuvastada ka muid bioloogilisi sidemeid, sealhulgas \u00f5dede-vendade v\u00f5i vanavanemate sugulust. Bioloogiliste sugulussuhete testid p\u00f5hinevad testitud isikute alleelide v\u00e4\u00e4rtuste ja populatsioonis esinevate alleelide sageduste matemaatilisel v\u00f5rdlusel.<\/p><p>Isaduse testimisel on osapooled v\u00e4idetav isa ja laps(ed). \u00dcldiselt p\u00e4rib laps oma vanematelt igas DNA-lokatsioonis kaks alleeli, \u00fche emalt ja teise isalt, nii et isaduse v\u00f5i emaduse kinnitamiseks peavad laps ja vanem jagama \u00fchte alleeli igas testitud lokatsioonis. Ema proovi kaasamine isaduse testimisse v\u00f5ib isaduse t\u00f5en\u00e4osust oluliselt suurendada, kuna on v\u00f5imalik kindlaks teha isalt p\u00e4ritud DNA alleelid. Ilma ema proovi kaasamiseta on uuringud n\u00e4idanud, et isaduse valepositiivsete hinnangute esinemissagedus on suurem. Sellisel juhul ei pruugi lapse ja testitud mehe \u00fchised alleelid p\u00e4ritud olla tegelikult konkreetselt testitud isalt, vaid v\u00f5ivad tegelikult p\u00e4ritud olla emalt, nii et isalt bioloogiliselt p\u00e4ritud alleel ei pruugi konkreetsel mehel olemas olla ja testitud mees ei pruugi bioloogiliselt olla lapse isa.<\/p><p>Isaduse testimisel v\u00f5rreldakse oletatava isa ja lapse alleele teatud DNA-piirkondades. Testi tulemus v\u00e4listab v\u00f5i kinnitab isaduse. Positiivne tulemus n\u00e4itab, et v\u00e4hemalt 99,99% t\u00f5en\u00e4osusega on tegemist lapse bioloogilise isaga. Negatiivne tulemus n\u00e4itab 100% t\u00f5en\u00e4osusega, et bioloogiline isadus on v\u00e4listatud. Testitulemusi ei saa kasutada kohtumenetluses, kuna prooviv\u00f5tmine ei ole kontrollitav, v\u00e4lja arvatud juhul, kui k\u00f5iki isikuid testitakse samal ajal kohapeal ja nende isik tuvastatakse isikut t\u00f5endava dokumendi abil.<\/p><p>Teaduslikud uuringud on n\u00e4idanud, et sugurakkude DNAs v\u00f5ivad tekkida muutused (mutatsioonid), mis kanduvad edasi j\u00e4rglastele. Geneetiliste testide puhul t\u00e4hendab see, et tuvastatud alleelid v\u00f5ivad pikeneda v\u00f5i l\u00fcheneda, st arvuline v\u00e4\u00e4rtus, mida me aruandes n\u00e4itame, muutub \u00fchest lookusest teise. Mutatsioonisagedused varieeruvad DNA piirkondade vahel ja on tuvastamisel kasutatud lookuste puhul alla 1% (n\u00e4iteks TH01 lookuste mutatsioonisagedus isasliini puhul on 0,009%, D3S1358 lookuste mutatsioonisagedus on 0,13%, D18S51 lookuste mutatsioonisagedus on 0,22% ja FGA lookuste mutatsioonisagedus on 0,32%). See t\u00e4hendab, et spermatosoidide moodustamise ajal v\u00f5ivad DNAs toimuda juhuslikud muutused, mille tulemusel isa ja laps ei jaga teatud DNA-lokatsioonis alleeli.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2515\" class=\"elementor-tab-title\" data-tab=\"5\" role=\"button\" aria-controls=\"elementor-tab-content-2515\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">K: Miks ei j\u00f5ua e-kirjad minuni?<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2515\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"5\" role=\"region\" aria-labelledby=\"elementor-tab-title-2515\"><p>Automaatsete e-postifiltrite t\u00f5ttu ei j\u00f5ua k\u00f5ik kirjad kohale. Kui lisate meie domeeniaadressi teie poolt heakskiidetud saatjate nimekirja (Valgesse nimekirja lisamine ehk<i data-stringify-type=\"italic\">\u00a0Whitelisting<\/i>) tagate, et saatja kirjad ei satuks r\u00e4mpsposti. Valgesse nimekirja lisamine pole keeruline ja v\u00f5tab juhiste j\u00e4rgi tehes k\u00f5igest m\u00f5ne minuti. Allpool leiate juhendid erinevatele e-posti teenusepakkujatele. Selleks, et meid nimekirja kanda, v\u00f5ite j\u00e4rgida allpool toodud juhiseid v\u00f5i v\u00f5tta \u00fchendust oma v\u00f5rguadministraatori ja\/v\u00f5i IT-toega ning paluda, et meie domeenist (@genorama.com) saabuvad e-kirjad kantaks valgesse nimekirja.<\/p><p><strong>E-kirjade kandmine valgesse nimekirja<\/strong><\/p><ul><li><strong>Outlookis<\/strong>\u00a0Vali aken \u201cHome\u201d v\u00f5i \u201cKodu\u201d Vali R\u00e4mpspost (Junk) \u2013&gt; R\u00e4mpsposti seaded (Junk Email Options) R\u00e4mpsposti seadetes leia Turvaliste Saatjate lahter ning vajuta \u201cLisa\u201d. Inglise keeles \u201cJunk Email Options\u201d ja \u201cSafe Senders\u201d, seej\u00e4rel vajutada \u201cAdd\u201d. Lisa aadress v\u00f5i domeen reale kirjuta kas @genorama.com v\u00f5i genorama.com. Seej\u00e4rel vajuta OK, et salvestada.<\/li><li><strong>Outlooki mobiilirakenduses<\/strong>\u00a0Ava rakendus. Vajuta kirjale mida soovid nimekirja lisada. Vajuta kolmele t\u00e4pile \u00fcleval nurgas. Vajuta \u201cLiiguta fookuses kausta\u201d (\u201cMove to focused folder\u201d) Kui uus aken avaneb, siis vali \u201cLiiguta see ning k\u00f5ik tulevased kirjad\u201d.<\/li><li><strong>Gmailis<\/strong>\u00a0Gmailis nimekirja kandmine k\u00e4ib kiirelt l\u00e4bi nende veebilehe: Vajuta seadete nupule (Ekraani \u00fcleval paremas nurgas), seej\u00e4rel vali \u201cSeaded\u201d tekkivast men\u00fc\u00fcst. Leia lahter \u201cFiltreeritud ja blokeeritud aadressid\u201d (\u201cFiltered and Blocked Addresses\u201d) Vali \u201cLoo uus filter\u201d ning lisa emailid v\u00f5i domeenid mida soovid valgesse nimekirja lisada. Et meie kirjad teieni j\u00f5uaksid, siis lisage ainult domeen ehk \u201c@genorama.com\u201d Vali \u201cLoo filter\u201d et kinnitada uus filter, seej\u00e4rel valige linnuke \u201c\u00c4ra suuna r\u00e4mpsposti\u201d.<\/li><li><strong>Gmaili mobiilirakenduses<\/strong>\u00a0Ava Gmaili rakendus. Leia ja ava r\u00e4mpsposti kaust. Vali meie saadetud e-kiri. Vali \u201cM\u00e4\u00e4ra mitte r\u00e4mpspostiks\u201d. N\u00fc\u00fcd j\u00f5uavad saatja kirjad teie postkasti.<\/li><li><strong>Hotmailis<\/strong>\u00a0Sisene enda Hotmaili kasutajasse, vajuta seadete ikoonile paremal \u00fcleval \u00e4\u00e4res, vali \u201cRohkem meilide seadeid\u201d (\u201cMore Mail Settings\u201d) Vali \u201cTurvalised ja blokeeritud saatjad\u201d Vali \u201cTurvalised saatjad\u201d Et k\u00f5ik meie kirjad j\u00f5uaksid Teieni lisa nimekirja \u201c@genorama.com\u201d vajutades nupule \u201cLisa\u201d. Genorama e-posti aadressidelt saabuvad kirjad ei satu enam r\u00e4mpsposti.<\/li><\/ul><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2516\" class=\"elementor-tab-title\" data-tab=\"6\" role=\"button\" aria-controls=\"elementor-tab-content-2516\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">K: Milliseid geeniteste leidub?<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2516\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"6\" role=\"region\" aria-labelledby=\"elementor-tab-title-2516\"><p><strong>Diagnostilisi teste<\/strong> kasutatakse selleks, et t\u00e4pselt kindlaks teha, milline haigus inimest haigestab. Diagnostilise testi tulemused v\u00f5ivad aidata teil teha valikuid, kuidas oma tervist ravida v\u00f5i hallata.<\/p><p><strong>Ennetavaid ja s\u00fcmptomitele eelnevaid geneetilisi teste<\/strong> kasutatakse selleks, et leida geenimuutusi, mis suurendavad inimese t\u00f5en\u00e4osust haiguste tekkeks. Nende testide tulemused annavad teile teavet teie riski kohta haigestuda konkreetsesse haigusse. Selline teave v\u00f5ib olla kasulik teie elustiili ja tervishoiu kohta tehtavate otsuste tegemisel.<\/p><p><strong>Kandjate teste<\/strong> kasutatakse selleks, et leida inimesi, kes \u201ekannavad\u201c haigusega seotud geenimuutust. Kandjatel ei pruugi ilmneda haiguse tunnuseid, kuid neil on siiski v\u00f5imalus anda geenimuutus edasi oma lastele, kes v\u00f5ivad haigust p\u00f5deda v\u00f5i saada ise kandjateks. M\u00f5nede haiguste puhul on haiguse tekkimiseks vaja, et geenimuutus p\u00e4rineks m\u00f5lemalt vanemalt. Seda t\u00fc\u00fcpi testimist pakutakse tavaliselt inimestele, kellel on perekonnas esinenud konkreetne p\u00e4rilik haigus v\u00f5i kes kuuluvad teatavatesse etnilistesse r\u00fchmadesse, kellel on suurem risk konkreetsete p\u00e4rilike haiguste tekkeks.<\/p><p><strong>S\u00fcnnieelset testimist<\/strong> pakutakse raseduse ajal, et aidata tuvastada looteid, kellel on teatavad haigused.<\/p><p><strong>Vasts\u00fcndinute s\u00f5eluuringut<\/strong> kasutatakse \u00fcks v\u00f5i kaks p\u00e4eva p\u00e4rast s\u00fcndi, et teha kindlaks, kas neil on teatud haigusi, mis teadaolevalt p\u00f5hjustavad tervise- ja arenguprobleeme.<\/p><p><strong>Farmakogenoomiline testimine<\/strong> annab teavet selle kohta, kuidas teatud ravimeid inimese keha t\u00f6\u00f6tleb. Seda t\u00fc\u00fcpi testid v\u00f5ivad aidata teie tervishoiuteenuse osutajal valida ravimid, mis sobivad teie geneetilise koostise suhtes k\u00f5ige paremini.<\/p><p><strong>Uurimisgeneetilisi teste<\/strong> kasutatakse selleks, et saada rohkem teavet geenide panuse kohta tervisesse ja haigustesse. M\u00f5nikord ei pruugi tulemused olla osalejatele otseselt kasulikud, kuid need v\u00f5ivad olla kasulikud teistele, aidates teadlastel laiendada oma arusaamist inimkehast, tervisest ja haigustest.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2517\" class=\"elementor-tab-title\" data-tab=\"7\" role=\"button\" aria-controls=\"elementor-tab-content-2517\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">Geneetiliste testide terminoloogia<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2517\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"7\" role=\"region\" aria-labelledby=\"elementor-tab-title-2517\"><p>Loodetavasti leiad allpool otsitava termini selgituse.<\/p><p><strong>Alleel:<\/strong> \u00fcks geeni v\u00f5imalikest vormidest.<\/p><p><strong>Autosoomne:<\/strong> omadus v\u00f5i seisund, mida p\u00f5hjustab geen \u201eautosoomil\u201c, st kromosoomidel 1 kuni 22 asuvas kromosoomis. Teisis\u00f5nu, omadus, mis ei ole seotud X- v\u00f5i Y-kromosoomiga. Autosoomsete geneetiliste seisundite n\u00e4ited on j\u00e4rgmised: Ts\u00fcstiline fibroos ja sirprakuline aneemia.<\/p><p><strong>Healoomuline variant:<\/strong> DNA muutus, mis ei m\u00f5juta geeni funktsiooni ega p\u00f5hjusta terviseprobleemi. Meil k\u00f5igil on palju healoomulisi variante, mis muudavad meid \u00fcksteisest ainulaadseks ja mis ei p\u00f5hjusta meditsiinilisi probleeme.<\/p><p><strong>P\u00f5sekaape proov:<\/strong> viis DNA kogumiseks inimese p\u00f5se sisek\u00fclje rakkudest, kas s\u00fcljeproovi v\u00f5i p\u00f5seproovi kaudu.<\/p><p><strong>Kandjate testimine\/seire:<\/strong> meditsiiniline test, mida tavaliselt tehakse pereplaneerimise eesm\u00e4rgil ja mis aitab tulevastel vanematel teada saada, kas nad on teatavate p\u00e4rilike geneetiliste haiguste kandjad, ja kui neil on \u00fchised kandjate haigused, kas nende lapsed v\u00f5ivad olla riskir\u00fchma kuuluvad.<\/p><p><strong>CGC (sertifitseeritud geneetiline n\u00f5ustaja):<\/strong><\/p><p><strong>CGC (Certified Genetic Counselor):<\/strong> Ameerika \u00dchendriikide geneetiliste n\u00f5ustajate kutsetunnistus, mille nad saavad p\u00e4rast eksami sooritamist, mis n\u00e4itab nende oskusi ja teadmisi tervishoiut\u00f6\u00f6tajana.<\/p><p><strong>Chorionic villus sampling (CVS):<\/strong> test, mille k\u00e4igus v\u00f5etakse raseduse alguses platsentast rakke, et avastada loote geneetilisi haigusi.<\/p><p><strong>Kromosoom:<\/strong> DNA on pakendatud struktuuridesse, mida nimetatakse kromosoomideks ja mida leidub elusolendite rakkudes. Inimesel on 46 kromosoomi, mis paiknevad 23 paarina. Esimesed on nummerdatud 1-22 ja neid nimetatakse \u201eautosoomideks\u201c. Viimast kromosoomipaari nimetatakse sugukromosoomideks: naistel on tavaliselt XX kromosoomid ja meestel tavaliselt XY kromosoomid.<\/p><p><strong>DNA:<\/strong> igas meie rakus sisalduv elu ehitusplokk, mis kannab meie geneetilist teavet.<\/p><p><strong>Diagnostiline testimine:<\/strong> meditsiiniline test, mis annab teavet, mis v\u00f5imaldab arstil diagnoosida haiguse.<\/p><p><strong>DNA-testimine:<\/strong> geneetilise testi vorm, mis anal\u00fc\u00fcsib konkreetselt DNA-d. Seda t\u00fc\u00fcpi teste v\u00f5ib kasutada haigust p\u00f5hjustada v\u00f5ivate DNA-muutuste tuvastamiseks v\u00f5i teha seda selleks, et saada teada muud geneetilist teavet isiku kohta, n\u00e4iteks isaduse v\u00f5i p\u00f5lvnemise kohta.<\/p><p><strong>Otse tarbijatele suunatud testimine:<\/strong> neid nimetatakse ka koduseks DNA-testimiseks v\u00f5i DTC-testimiseks, need on testid, mida turustatakse otse tarbijatele ja mis v\u00f5imaldavad neil osta mitmesuguseid geneetilisi teste ja saada tulemusi ilma isikliku arsti v\u00f5i kindlustusfirma kaasamiseta.<\/p><p><strong>Eksoom:<\/strong> DNA osa, mis sisaldab geene, mis moodustab umbes 1-2% kogu meie DNAst.<\/p><p><strong>Geen:<\/strong> DNA l\u00f5ik, mis sisaldab konkreetset juhist keha jaoks. See \u00fctleb kehale, kuidas teha valku, mis on keha ehitusplokk. Geenid on p\u00e4rilikud ja m\u00e4\u00e4ravad ka inimese omadused, n\u00e4iteks silmav\u00e4rvi v\u00f5i selle, kas tal on teatud geneetilised haigused v\u00f5i mitte.<\/p><p><strong>Geneetiline n\u00f5ustaja:<\/strong> tervishoiut\u00f6\u00f6taja, kellel on geneetika ja n\u00f5ustamise alane koolitus ja kes t\u00f6\u00f6tab koos arstide, meditsiini\u00f5dede v\u00f5i teiste teie tervishoiumeeskonna liikmetega. Geneetilised n\u00f5ustajad hindavad teie haiguslugu ja perekonna ajalugu, et teha kindlaks, kas teil on geneetilise v\u00f5i p\u00e4riliku haiguse risk, ning arutavad olemasolevate geneetiliste testimisv\u00f5imaluste m\u00f5ju.<\/p><p><strong>Geneetiline risk:<\/strong> meie geenide osa t\u00f5en\u00e4osuses, et meil tekib teatud haigus v\u00f5i seisund.<\/p><p><strong>Geneetiline testimine:<\/strong> inimese geneetilise materjali (st kromosoomide v\u00f5i geenide) anal\u00fc\u00fcsimine, et tuvastada muutused, mis v\u00f5ivad p\u00f5hjustada geneetilist haigust v\u00f5i eelsoodumust.<\/p><p><strong>Genot\u00fc\u00fcp:<\/strong> kirjeldab teie geneetilist koostist. Seda terminit kasutatakse tavaliselt siis, kui viidatakse konkreetsele tunnusele.<\/p><p><strong>Sugupoolte testimine:<\/strong> tavaliselt tehakse vere- v\u00f5i s\u00fcljeprooviga, et otsida p\u00e4rilikke geneetilisi muutusi v\u00f5i muutusi, mis on kellelgi juba s\u00fcnnist saadik olemas ja mis v\u00f5ivad kanduda edasi \u00fchest p\u00f5lvkonnast teise.<\/p><p><strong>Teavitatud n\u00f5usolek:<\/strong> protsess, mille k\u00e4igus saadakse teada olulised \u00fcksikasjad meditsiinilise ravi (nt ravim, operatsioon v\u00f5i test) kohta, et oleks v\u00f5imalik otsustada, kas ravi v\u00f5i testi teha v\u00f5i mitte.<\/p><p><strong>T\u00f5en\u00e4oliselt patogeenne variant:<\/strong> DNA muutus, mis meie arvates t\u00f5en\u00e4oliselt p\u00f5hjustab, et geen ei toimi ja v\u00f5ib p\u00f5hjustada terviseprobleemi. Tavaliselt on teadlased ja arstid 90% ulatuses kindlad, et need p\u00f5hjustavad haigust, kuid veel ei ole kogutud piisavalt t\u00f5endeid, et olla 100% kindel.<\/p><p><strong>Mutatsioon (geneetiline mutatsioon):<\/strong> DNA muutumine algsest seisundist. M\u00f5ned mutatsioonid ei p\u00f5hjusta mingeid probleeme, samas kui teised p\u00f5hjustavad haigusi; seda terminit kasutatakse siiski k\u00f5ige sagedamini, kui inimesel on geneetiline muutus, mis p\u00f5hjustab terviseh\u00e4ireid.<\/p><p><strong>Patogeenne variant:<\/strong> muutus DNAs, mis teadaolevalt p\u00f5hjustab, et geen ei t\u00f6\u00f6ta ja v\u00f5ib p\u00f5hjustada terviseprobleemi.<\/p><p><strong>Personaalne meditsiin:<\/strong> m\u00f5iste, mida kasutatakse uue tervishoiualase l\u00e4henemise kirjeldamiseks, mis kohandab haiguste ennetamist ja\/v\u00f5i ravi inimese geenide, keskkonna, elustiili ja muude tegurite alusel.<\/p><p><strong>Preimplantatsiooniline geneetiline testimine (PGT):<\/strong> in vitro viljastamise (IVF) k\u00e4igus tehtav s\u00f5eltest. Neid on kolme liiki: PGT-M, PGT-SR ja PGT-A, millest iga\u00fcks h\u00f5lmab embr\u00fco testimist teatavate geneetiliste seisundite (nt ts\u00fcstiline fibroos v\u00f5i Downi s\u00fcndroom) suhtes. Seda t\u00fc\u00fcpi testimist nimetati varem implantaadieelseks geneetiliseks diagnostikaks (PGD).<\/p><p><strong>Retsessiivne:<\/strong> geeni vorm, mis on maskeeritud geeni alternatiivse (domineeriva) vormiga ja v\u00e4ljendub ainult siis, kui inimesel on kaks sellist mittedomineerivat (retsessiivset) koopiat. Seda nimetatakse ka retsessiivseks alleeliks.<\/p><p><strong>Sekveneerimine:<\/strong> test, mis loeb DNA-koodi t\u00e4htede kaupa l\u00e4bi, et otsida muutusi, mis v\u00f5ivad p\u00f5hjustada terviseprobleeme. Seda testi v\u00f5ib teha \u00fche geeni, geenipaneeli v\u00f5i isegi suurema osa DNA-st (genoomi v\u00f5i eksoomi).<\/p><p><strong>X-koodiga seotud:<\/strong> X-kromosoomil asuva geeni p\u00f5hjustatud tunnus v\u00f5i seisund.<\/p><p><strong>SNP (single nucleotide polymorphism) testimine:<\/strong> testimine, mille k\u00e4igus otsitakse DNA-s olevaid \u00fche t\u00e4he muutusi. (See erineb kogu geeni v\u00f5i genoomi sekveneerimisest).<\/p><p><strong>Kasvaja\/somaatiline testimine:<\/strong> testimine, mida tehakse kasvaja v\u00f5i v\u00e4hi rakkudega, et otsida DNA muutusi. Kasvaja DNA-profiili tundmine v\u00f5ib aidata arstidel kohandada ravi. Enamik kasvaja DNA-muutusi ei ole p\u00e4rilik ja neid ei esine inimese tervetel rakkudel.<\/p><p><strong>Variant:<\/strong> muutus teie DNA juhistes (nagu muutus s\u00f5na \u00f5igekirjas), mis erineb sellest, mis on enamikul inimestel. See v\u00f5ib muuta v\u00f5i mitte muuta geeni toimimist.<\/p><p><strong>VUS (Variant of Uncertain\/Unknown Significance):<\/strong> muutus DNA juhistes, mille puhul teadlased ja arstid ei ole veel kindlad, kas see p\u00f5hjustab terviseprobleeme.<\/p><p>\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-toggle-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2518\" class=\"elementor-tab-title\" data-tab=\"8\" role=\"button\" aria-controls=\"elementor-tab-content-2518\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon elementor-toggle-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-closed\"><i class=\"fas fa-caret-right\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-toggle-icon-opened\"><i class=\"elementor-toggle-icon-opened fas fa-caret-up\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-toggle-title\" tabindex=\"0\">Unetesti lisainfo<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\t<div id=\"elementor-tab-content-2518\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"8\" role=\"region\" aria-labelledby=\"elementor-tab-title-2518\"><h3 data-start=\"258\" data-end=\"291\"><strong data-start=\"265\" data-end=\"291\">Une geenitestiga saad teada enda unemustri ise\u00e4rasused t\u00e4nu PER-3 geeni anal\u00fc\u00fcsile.<\/strong><\/h3><p>PER-3 (Period Circadian Regulator 3) geen on \u00fcks inimese tsirkadiaanr\u00fctme ehk \u00f6\u00f6p\u00e4evar\u00fctme reguleerivatest geenidest. See kuulub PER-geenide perekonda koos PER1 ja PER2 geenidega ning m\u00e4ngib rolli keha sisemise kella (bioloogilise kella) t\u00f6\u00f6s.<\/p><p><strong>PER-3 geeni funktsioon<\/strong><\/p><p>PER3 geen kodeerib PER3 valku, mis osaleb:<\/p><ul><li>\u00d6\u00f6p\u00e4evar\u00fctmi ehk tsirkadiaalse r\u00fctmi\u00a0reguleerimises \u2014 see on keha sisemine mehhanism, mis reguleerib une-\u00e4rkveloleku ts\u00fcklit, kehatemperatuuri, hormoonide taset ja muid \u00f6\u00f6p\u00e4evaseid r\u00fctme.<\/li><li>Negatiivses tagasisideahelas, mis hoiab tsirkadiaanset kella tasakaalus. PER3 valk seondub teiste tsirkadiaanvalkudega (nt CLOCK, BMAL1, PER1, PER2, CRY1\/2), et pidurdada enda ja teiste geenide transkriptsiooni, sulgedes seel\u00e4bi tagasisideahela.<\/li><\/ul><p><strong>Seos une ja k\u00e4itumisega<br \/><\/strong><br \/>PER3 geenis on teada pol\u00fcmorfism (muutuv DNA korduste arv), mis m\u00f5jutab uneharjumusi:<\/p><ul><li><strong>PER3 4\/4 (l\u00fchike alleel):<br \/><\/strong>seotud parema taluvusega unevaeguse korral, esineb sagedamini &#8220;<strong>\u00f6\u00f6kullidel<\/strong>&#8220;.<\/li><li><strong>PER3 5\/5 (pikk alleel):<br \/><\/strong>seotud varajase kronot\u00fc\u00fcbiga (&#8220;<strong>hommikuinimesed<\/strong>&#8220;) ning suurenenud tundlikkusega unepuuduse korral (nt kognitiivne langus p\u00e4rast magamata \u00f6\u00f6d).<\/li><li><p data-start=\"42\" data-end=\"378\"><strong data-start=\"42\" data-end=\"81\">PER3 4\/5 (heteros\u00fcgootne genot\u00fc\u00fcp):<\/strong><br data-start=\"81\" data-end=\"84\" \/>T\u00e4histab <strong data-start=\"93\" data-end=\"119\">vahepealset kronot\u00fc\u00fcpi<\/strong>, mille tunnused j\u00e4\u00e4vad hommiku- ja \u00f5htuinimese vahele. Selle genot\u00fc\u00fcbiga inimestel on <strong data-start=\"206\" data-end=\"247\">m\u00f5\u00f5dukas tundlikkus unepuuduse suhtes<\/strong> ning <strong data-start=\"253\" data-end=\"280\" data-is-only-node=\"\">keskmine kohanemisv\u00f5ime<\/strong> uneaja muutustega, n\u00e4idates <strong data-start=\"309\" data-end=\"340\">tasakaalustatud reaktsiooni<\/strong> v\u00f5rreldes PER3 4\/4 ja 5\/5 \u00e4\u00e4rmustega.<\/p><\/li><\/ul><p><strong>Kliiniline ja teaduslik t\u00e4hendus<br \/><\/strong><br \/>PER3 pol\u00fcmorfisme uuritakse seoses uneh\u00e4irete, \u00f6\u00f6p\u00e4evar\u00fctmih\u00e4irete (nt hiline une-\u00e4rkveloleku faasih\u00e4ire) ja isegi meeleoluh\u00e4iretega (nt depressioon).<\/p><p>Samuti on m\u00f5ned uuringud leidnud seoseid PER3 varieeruvuse ja kognitiivsete v\u00f5imete k\u00f5ikumisega unev\u00f5lgades.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Korduma Kippuvad K\u00fcsimused Kui te ei leia vastust oma k\u00fcsimusele allpool, v\u00f5tke meiega \u00fchendust. K: Kuidas tellida ja registreerida oma testi? K: Kuidas tellida testi? Oma testi tellimiseks valige lihtsalt soovitud test veebilehe \u00fclaosas olevast poe men\u00fc\u00fcst, kasutage kontaktivormi v\u00f5i saatke meile e-kiri aadressil \u201einfo@genorama.com\u201c. Lisateavet erinevate testide kohta saate lugeda, kui kl\u00f5psate kataloogist neile. [&hellip;]<\/p>\n","protected":false},"author":7,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"_acf_changed":false,"ocean_post_layout":"","ocean_both_sidebars_style":"","ocean_both_sidebars_content_width":0,"ocean_both_sidebars_sidebars_width":0,"ocean_sidebar":"","ocean_second_sidebar":"","ocean_disable_margins":"enable","ocean_add_body_class":"","ocean_shortcode_before_top_bar":"","ocean_shortcode_after_top_bar":"","ocean_shortcode_before_header":"","ocean_shortcode_after_header":"","ocean_has_shortcode":"","ocean_shortcode_after_title":"","ocean_shortcode_before_footer_widgets":"","ocean_shortcode_after_footer_widgets":"","ocean_shortcode_before_footer_bottom":"","ocean_shortcode_after_footer_bottom":"","ocean_display_top_bar":"default","ocean_display_header":"default","ocean_header_style":"","ocean_center_header_left_menu":"","ocean_custom_header_template":"","ocean_custom_logo":0,"ocean_custom_retina_logo":0,"ocean_custom_logo_max_width":0,"ocean_custom_logo_tablet_max_width":0,"ocean_custom_logo_mobile_max_width":0,"ocean_custom_logo_max_height":0,"ocean_custom_logo_tablet_max_height":0,"ocean_custom_logo_mobile_max_height":0,"ocean_header_custom_menu":"","ocean_menu_typo_font_family":"","ocean_menu_typo_font_subset":"","ocean_menu_typo_font_size":0,"ocean_menu_typo_font_size_tablet":0,"ocean_menu_typo_font_size_mobile":0,"ocean_menu_typo_font_size_unit":"px","ocean_menu_typo_font_weight":"","ocean_menu_typo_font_weight_tablet":"","ocean_menu_typo_font_weight_mobile":"","ocean_menu_typo_transform":"","ocean_menu_typo_transform_tablet":"","ocean_menu_typo_transform_mobile":"","ocean_menu_typo_line_height":0,"ocean_menu_typo_line_height_tablet":0,"ocean_menu_typo_line_height_mobile":0,"ocean_menu_typo_line_height_unit":"","ocean_menu_typo_spacing":0,"ocean_menu_typo_spacing_tablet":0,"ocean_menu_typo_spacing_mobile":0,"ocean_menu_typo_spacing_unit":"","ocean_menu_link_color":"","ocean_menu_link_color_hover":"","ocean_menu_link_color_active":"","ocean_menu_link_background":"","ocean_menu_link_hover_background":"","ocean_menu_link_active_background":"","ocean_menu_social_links_bg":"","ocean_menu_social_hover_links_bg":"","ocean_menu_social_links_color":"","ocean_menu_social_hover_links_color":"","ocean_disable_title":"default","ocean_disable_heading":"default","ocean_post_title":"","ocean_post_subheading":"","ocean_post_title_style":"","ocean_post_title_background_color":"","ocean_post_title_background":0,"ocean_post_title_bg_image_position":"","ocean_post_title_bg_image_attachment":"","ocean_post_title_bg_image_repeat":"","ocean_post_title_bg_image_size":"","ocean_post_title_height":0,"ocean_post_title_bg_overlay":0.5,"ocean_post_title_bg_overlay_color":"","ocean_disable_breadcrumbs":"default","ocean_breadcrumbs_color":"","ocean_breadcrumbs_separator_color":"","ocean_breadcrumbs_links_color":"","ocean_breadcrumbs_links_hover_color":"","ocean_display_footer_widgets":"default","ocean_display_footer_bottom":"default","ocean_custom_footer_template":"","footnotes":""},"class_list":["post-6339","page","type-page","status-publish","hentry","entry","owp-thumbs-layout-horizontal","owp-btn-normal","owp-tabs-layout-horizontal","has-no-thumbnails","has-product-nav"],"acf":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/pages\/6339","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/users\/7"}],"replies":[{"embeddable":true,"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/comments?post=6339"}],"version-history":[{"count":10,"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/pages\/6339\/revisions"}],"predecessor-version":[{"id":7338,"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/pages\/6339\/revisions\/7338"}],"wp:attachment":[{"href":"https:\/\/genorama.com\/et\/wp-json\/wp\/v2\/media?parent=6339"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}