DNA Genetic Testing & Analyse - 23andMe AU, DE, FR & EU

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DNAGeneticTestingForHealth,AncestryAndMore-23andMe(function(){'usestrict';window.optimizely=window.optimizely||[];window.optimizely.push({type:"holdEvents"});window.addEventListener("load",function(){window.optimizely.push({type:"sendEvents"});});})();window.heap=window.heap||[],heap.load=function(e,t){window.heap.appid=e,window.heap.config=t=t||{};varr=t.forceSSL||":"===document.location.protocol,a=document.createElement("script");a.type="text/jascriDNA Genetic Testing & Analyse - 23andMe AU, DE, FR & 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e-causingvariants.PhoneSlide0:Next-GenerationSequencingPhoneSlide1:BiannualBloodTestingPhoneSlide2:Genetics-informedClinicalCareLearnmore23ANDME+PREMIUM190+personalizedgenotypingreportswithnewreportsandfeaturesdeliveredthroughouttheyear.LearnmoreCancerReportsPoweredby23andMeResearchPremiumreportstohelpyoulearnmoreaboutbreastcancer(femalesonly),prostatecancer(malesonly),colorectalcancer(certainethnicities)andskincancer.PhoneSlide0:CancerReportsPhoneSlide1:PharmacogeneticsReportsPhoneSlide2:HealthActionPlanLearnmoreHEALTH+ANCESTRYSERVICELearnwhatyourDNAcantellyouaboutyourhealthandancestry.LearnmoreFamilyHealthHistoryTreeOptintoeasilyinput,trackanddownloadyourfamilyhealthhistorytosharewithyourhealthcareprovider.PhoneSlide0:FamilyHealthHistoryTreePhoneSlide1:HealthPredispositionsPhoneSlide2:CarrierStatusReportsLearnmoreANCESTRYSERVICEThemostcomprehensiveancestrybreakdownonthemarketwithover3,000regions.LearnmoreAncestryCompositionDiscoverwhereintheworldyourDNAisfromacross3000+regions—insomecases,downtothecountylevel.PhoneSlide0:AncestryCompositionPhoneSlide1:FamilyTreePhoneSlide2:DNARelativeFinderLearnmoreWhichservicewillyoustartwithtoday?Remember,youcanalwaysupgradewithouthingDNA Genetic Testing & Analyse - 23andMe AU, DE, FR & EUtospitain.SelectfirstservicetocompareAncestryService23andMe+Premium23andMe+TotalHealthSelectsecondservicetocompareHealth+AncestryService23andMe+Premium23andMe+TotalHealthFeatureAncestryServiceHealth+plusAncestryServiceAncestryServiceOriginalPrice:$119SalePrice:$59Addtocart-ancestryHealth+plusAncestryService$199Addtocart-healthImportanttestinfoGenotypingreportsGenotypingexaminesDNAvariantsatcertainpre-identifiedpositionsinthegenome.Thespecificvariantswelookatgenerallyprovidecovereofcommonlyknownvariationsacrosstheentiregenome.80+150+ExomeSequencingReportsΔLearnaboutImportantInformationforTotalhealthExomesequencingisanadvancedgenetictestingtechniquethatfocusesondecodingtheexomeofanindividualx27;sgenome.Theexomerepresentstheprotein-codingregionsofgenes,whichmakeuponlyabout2%oftheentiregenomebutcontainthemajorityofgeneticvariantsassociatedwithdiseaserisk.AncestryandTraitReportsDNARelativeFinderandFamilyTree(Optin)HealthPredispositionreports*LearnaboutConsiderationsandLimitationsforHealthPredispositionsReports,CarrierStatusReportsandGeneticHealthRisksLearnhowyourgeneticscaninfluenceyourchancesofdevelopingcertainhealthconditions.10+CarrierStatusreports*LearnaboutConsiderationsandLimitationsforHealthPredispositionsReports,CarrierStatusReportsandGeneticHealthRisksIfyouarestartingafamily,findoutifyouareacarrierforcertaininheritedconditions.WellnessreportsLearnhowyourgenesplayaroleinyourwell-beingandlifestylechoices.5+FamilyHealthHistoryTreeOptintoeasilyinput,trackanddownloadyourfamilyhealthhistorytosharewithyourhealthcareprovider.Pharmacogeneticsreports**LearnaboutConsiderationsandLimitationsforPharmacogeneticsReportsDiscoverhowyourDNAmayimpacthowyourbodyprocessescertainmedicationswiththreenewPharmacogeneticsreports.EnhancedancestryfeaturesGetadvancedfilteringforDNARelativeFinderandaccessupto5000DNArelatives.JustAddedHistoricalMatchesSMUncoveryourhistoricalandancientrelatives,linkingyoutothepast.Breast,ProstateandColorectalCancerreportsInsightsintoyourgeneticlikelihoodofdevelopingbreast(femalesonly),prostate(malesonly)andcolorectal(certainethnicities)cancer.allPoweredby23andMeResearchHealthTracksSMSeehowmakinghealthychoiceseachdaycangreatlyimpactyourhealthovertimeHealthActionPlanPersonalizedandongoingrecommendationsbasedongeneticandnon-geneticdata.OngoingnewreportsandfeaturesGetaccesstonewpremiumreportsandfeaturesthroughouttheyear.BloodTestingΔLearnaboutImportantInformationforTotalhealthEligibleparticipantsmayorderin-personbloodtestinginitiatedbyaclinicianandgetresultsinthe23andMeapp.Add-OnPurchaseJustAddedBiologicaleMonitorhowyourbodyisingphysiologicallybasedonkeybiomarkersandchangethetrajectoryofyourhealth.Genetics-informedclinicalcareΔLearnaboutImportantInformationforTotalhealthAccesstoclinicianswithtrainingingenetics.Includesunlimiteddirectmessing,plusadedicatedvirtualconsultationannually.PrivacyKnowthatyouareincontrolofyourDNA.Discoveryshouldnevercomeattheexpenseofprivacy.Yourdataisencrypted,protectedandunderyourcontrol.Youdecidewhatyouwanttoknowandwhatyouwanttoshare.LearnmoreaboutprivacyLearnmoreaboutprivacyResearchKnowyou’remakingadifference.Whenyouoptintoparticipateinourresearch,youjoinforceswithmillionsofotherpeoplecontributingtoscience.Yourparticipationcouldhelpleadtodiscoveriesthatmayonedaymakeanimpactonyourownhealth,thehealthofyourfamilyandultimately,peoplearoundtheworld.(Lookatyougo.)LearnmoreaboutresearchLearnmoreaboutresearchFrequentlyAskedQuestionsHowaccurateis23andMe?23andMehasrigorousstandardsthatensurehigh-qualityresults.Ourteamofscientistsandmedicalexpertsusearobustprocesstodevelopgeneticreportsforourcustomers.Herearespecificexamples:Withoneofthelargestreferencedatasetsintheworld,23andMeprovidescustomerswithoneofthemostdetailedandaccurateancestrybreakdownsonthemarket.Ouralgorithmsmakeancestryestimatesbasedonprobabilitiesandthey’regenerallyveryaccurate,butyourresultsarenotsetinstone.Wearealwaystryingtoimproveandrefinetheseestimates.OurGeneticHealthRisk*LearnaboutConsiderationsandLimitationsforHealthPredispositionsReports,CarrierStatusReportsandGeneticHealthRisks,CarrierStatus*LearnaboutConsiderationsandLimitationsforHealthPredispositionsReports,CarrierStatusReportsandGeneticHealthRisks,Pharmacogenetics**LearnaboutConsiderationsandLimitationsforPharmacogeneticsReportsreportsmeetFDArequirements.Thismeansthateachvariantinthosereportsdemonstrated>greaterthan99%accuracyandreproducibilitywhentestedunderdifferentlaboratoryconditions.Thisarticleontheaccuracyof23andMereportsprovidesadditionalinformation.Howdoes23andMeDNAtestingwork?Afteryouprovideasalivasample,23andMeusesgenotypingtoanalyzeyourDNA.Thismeanswelookatspecificlocationsinyourgenomethatareknowntodifferbetweenpeople.Wethenturnthoseresultsintopersonalizedgeneticreportsoneverythingfromancestrycompositiontotraitstogenetichealthrisks.NotethatgenotypingisdifferentfromDNAsequencing,whichlooksateveryletterinaparticularstretchofDNA.Whocanuse23andMe?Mostadultswhoareabletoprovidesalivasamplescanusethe23andMekit.HowevertherearesomeconsiderationsthatcancomplicatetheDNAaccuracy.CheckoutourTermsofServiceformoreinfoonthosecases.HowdoIgetmy23andMereportsandhowlongdoesittake?Tobegin,visit/start.OnceyouhesuccessfullyregisteredyourDNAtestingkit,providedasalivasampleandputthekitinthemail,youcanusethereturntrackinglinkailableonyourprofilehomepetotrackyourkitx27;sprogresstothelab.Onceyoursamplereachesthelab,itistypicallyprocessedwithinafewweeks,withresultsthendeliveredtoyoursecureonlineaccount.Do23andMeDNAtestkitsexpire?Weencourecustomerstoprovidetheirsamplebeforethe"Collectsalivaby"dateonthesideofthecollectiontube.Ifyoursamplecollectionkitislostordamed,orifithasexpired,pleasecontactcustomercaretoassistyouwithgettingareplacementkit.WhyshouldIchoose23andMe?TherearemanybenefitsofDNAtesting,includingfindingrelatives,learningwhetheryouhegeneticvariantsyoucouldpassontoyourchildren,andreceivingpersonalizedinsightsintoyourhealthandancestry.23andMeHealth+AncestryServiceoffers150+DNAreportsthatdojustthat.Inadditiontotakinggreatercontrolofyourownhealthanddiggingdeeperintoyourancestry,youcanalsooptintoparticipateinresearchthatcouldhelpfuelscientificdiscoveriesthatbenefitthelargercommunity.Wex27;realsocommittedtoprovidingyouwithasafeplacewhereyoucanlearnaboutyourDNAknowingyourprivacyisprotected.23andMehassold12+millionkits,andwitheachandeveryoneofthose,privacyhasbeenournumberonepriority.Youmaylearnmoreaboutourcommitmenttoprivacyhereonourprivacype.Stayintheknow.Keepup-to-datewithnewdiscoveriesandexclusivepromotionsonourDNAtestingkitsandservices.EmailAddressSignup*The23andMePGStestincludeshealthpredispositionandcarrierstatusreports.HealthpredispositionreportsincludebothreportsthatmeetFDArequirementsforgenetichealthrisksandreportswhicharebasedon23andMeresearchandhenotbeenreviewedbytheFDA.ThetestusesqualitativegenotypingtodetectselectclinicallyrelevantvariantsinthegenomicDNAofadultsfromsalivaforthepurposeofreportingandinterpretinggenetichealthrisksandreportingcarrierstatus.Itisnotintendedtodinoseanydisease.Yourethnicitymayaffecttherelevanceofeachreportandhowyourgenetichealthriskresultsareinterpreted.Eachgenetichealthriskreportdescribesifapersonhasvariantsassociatedwithahigherriskofdevelopingadisease,butdoesnotdescribeaperson’soverallriskofdevelopingthedisease.Thetestisnotintendedtotellyouanythingaboutyourcurrentstateofhealth,ortobeusedtomakemedicaldecisions,includingwhetherornotyoushouldtakeamedication,howmuchofamedicationyoushouldtake,ordetermineanytreatment.Ourcarrierstatusreportscanbeusedtodeterminecarrierstatus,butcannotdetermineifyouhetwocopiesofanygeneticvariant.Thesecarrierreportsarenotintendedtotellyouanythingaboutyourriskfordevelopingadiseaseinthefuture,thehealthofyourfetus,oryournewbornchildx27;sriskofdevelopingaparticulardiseaselaterinlife.Forcertainconditions,weprovideasinglereportthatincludesinformationonbothcarrierstatusandgenetichealthrisk.Warnings&Limitations:The23andMePGSGeneticHealthRiskReportforBRCA1/BRCA2(SelectedVariants)isindicatedforreportingof44variantsintheBRCA1andBRCA2genes.Thereportdescribesifapersonx27;sgeneticresultisassociatedwithanincreasedriskofdevelopingbreastcancerandovariancancerandmaybeassociatedwithanincreasedriskforprostatecancer,pancreaticcancer,andpotentiallyothercancers.ThevariantsincludedinthisreportdonotrepresentthemajorityoftheBRCA1/BRCA2variantsinpeopleofmostethnicities.Thisreportdoesnotincludevariantsinothergeneslinkedtohereditarycancersandtheabsenceofvariantsincludedinthisreportdoesnotruleoutthepresenceofothergeneticvariantsthatmayimpactcancerrisk.Thisreportisforover-the-counterusebyadultsovertheeof18,andprovidesgeneticinformationtoinformdiscussionswithahealthcareprofessional.ThePGStestisnotasubstituteforvisitstoahealthcareprofessionalforrecommendedscreeningsorappropriatefollow-up.Resultsshouldbeconfirmedinaclinicalsettingbeforetakinganymedicalaction.Forimportantinformationandlimitationsregardingeachgenetichealthriskandcarrierstatusreport,visit23andme.com/test-info/**23andMePGSPharmacogeneticsreports:The23andMetestusesqualitativegenotypingtodetect3variantsintheCYP2C19gene,2variantsintheDPYDgeneand1variantintheSLCO1B1geneinthegenomicDNAofadultsfromsalivaforthepurposeofreportingandinterpretinginformationabouttheprocessingofcertaintherapeuticstoinformdiscussionswithahealthcareprofessional.Itdoesnotdescribeifapersonwillorwillnotrespondtoaparticulartherapeutic.OurCYP2C19Pharmacogeneticsreportprovidescertaininformationaboutvariantsassociatedwithmetabolismofsometherapeuticsandprovidesinterpretivedruginformationregardingthepotentialeffectofcitalopramandclopidogreltherapy.OurSLCO1B1Pharmacogeneticsreportprovidescertaininformationaboutvariantsassociatedwiththeprocessingofsometherapeuticsandprovidesinterpretivedruginformationregardingthepotentialeffectofsimvastatintherapy.OurDPYDPharmacogeneticsreportdoesnotdescribetheassociationbetweendetectedvariantsandanyspecifictherapeutic.ResultsforDPYDandcertainCYP2C19resultsshouldbeconfirmedbyanindependentgenetictestprescribedbyyourownhealthcareproviderbeforetakinganymedicalaction.Warning:Testinformationshouldnotbeusedtostart,stop,orchangeanycourseoftreatmentanddoesnottestforallpossiblevariantsthatmayaffectmetabolismorproteinfunction.ThePGStestisnotasubstituteforvisitstoahealthcareprofessional.Makingchangestoyourcurrentregimencanleadtoharmfulsideeffectsorreducedintendedbenefitsofyourmedication,thereforeconsultwithyourhealthcareprofessionalbeforetakinganymedicalaction.ForimportantinformationandlimitationsregardingPharmacogeneticreports,visit23andme.com/test-info/pharmacogenetics/ΔtriangleExomeSequencingandbloodtestingservicesareailabletoeligiblecustomersuponcompletionoftheintakequestionnairethatmustbereviewed,approvedandorderedbyathird-partyclinician.ExomeSequencingisanalyzedbyaCLIA-andCAP-accreditedlaboratory.BloodtestingiscompletedbyQuestDinostics.AlltelehealthservicesareprovidedinaccordancewiththeTelehealthTermsandConsenttoTelehealth.FooterServicesHealth+plusAncestryAncestryService23andMe+plusPremium23andMe+plusTotalHealthGiftsMerchandiseCompanyInvestorsMediaCenterBlogCareersReferaFriendReturn&RefundPolicyCustomerCareFSA/HSAEligibilitySiteMapLearnAboutUsHowitWorksSciencePrivacyResearchStoriesSurnameDiscoveryDiversity,Equity&InclusionGeneticsLearningHubDNA&PersonalizedHealthcareLegalImportantTestInfoTermsofServicePrivacyStatementDataProtectionFamilyConsiderationsResearchConsentIndividualDataConsentBiobankingConsentCookiePolicyCookieChoicesPatentInformationReportaSecurityIssueConsumerHealthDataPrivacyPolicyPartnerWithUsHealthcareProfessionalsScientistsTherapeuticsBusinessDevelopmentDownloadAppUnitedStates|ChangeChangelocationConnect©202423andMe,Inc.Allrightsreserved.(function(){varpattern=/^DNA 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