23andMe Health+ Ancestry 150 genetic reports genes test dna family disease new

Description: 23andMe Health+ Ancestry Saliva Kit Exp 2022 prepaid no fee 150 reports fast This is for ONE KIT NOT 2, READ , 1 KIT genetic reports genes test dna family disease new Health test includes tests for genes such as BRCA which is linked to Breast cancer. alzheimers , organs . Plus finds close relatives you may not know about across the world. Add 1000s of DNA relatives in one test and reach them to find out about common ancestors. will send anywhere , no processing fee , free mailer, free results , no hidden fees This is good for 2 years, fresh kit just arrived !! Personal service for those overseas or unsure how to use this kit. Reports included in all services:NOW WITH 2000+ REGIONSAncestry Reports50+ reportsAncestry CompositionAncestry Detail Reports (48 reports)Family TreeMaternal HaplogroupPaternal HaplogroupNeanderthal AncestrySee sample report- AncestryTrait Reports30+ traitsAbility to Match Musical PitchAsparagus Odor DetectionBack Hair (available for men only)Bald Spot (available for men only)Bitter TasteBunionsCheek DimplesCilantro Taste AversionCleft ChinDandruffEarlobe TypeEarly Hair Loss (available for men only)Earwax TypeEye ColorFear of HeightsFear of Public SpeakingFinger Length RatioFlat FeetFrecklesHair Photobleaching (hair lightening from the sun)Hair TextureHair ThicknessIce Cream Flavor PreferenceLight or Dark HairMisophonia (hatred of the sound of chewing)Mosquito Bite FrequencyMotion SicknessNewborn HairPhotic Sneeze ReflexRed HairSkin PigmentationStretch MarksSweet vs. SaltyToe Length RatioUnibrowWake-Up TimeWidow's PeakSee sample report- TraitsReports included in Health + Ancestry Service and 23andMe+:Health Predisposition Reports*10+ reportsType 2 Diabetes ( Powered by 23andMe Research )Learn moreGenetic likelihood for a disorder of blood sugar regulation1,000+ variants in many genes; variants found in many ethnicitiesAge-Related Macular DegenerationGenetic risk for a form ofadult-onset vision loss2 variants in the ARMS2 and CFH genes; relevant for European descentAlpha-1 Antitrypsin DeficiencyGenetic risk for lung and liver disease2 variants in the SERPINA1 gene; relevant for European descentBRCA1/BRCA2 (Selected Variants)Learn moreGenetic risk based on a limited set of variants for breast, ovarian and other cancers3 variants in the BRCA1 and BRCA2 genes; relevant for Ashkenazi Jewish descentCeliac DiseaseGenetic risk for gluten-relatedautoimmune disorder2 variants near the HLA-DQB1 and HLA-DQA1 genes; relevant for European descentChronic Kidney Disease (APOL1-Related)Genetic risk for a form of chronic kidney disease2 variants in the APOL1 gene; relevant for African descentFamilial HypercholesterolemiaGenetic risk for very high cholesterol, which can increase the risk for heart disease24 variants in the LDLR and APOB genes; relevant for European, Lebanese, Old Order Amish descentG6PD DeficiencyGenetic risk for a form of anemia2 variants in the G6PD gene; relevant for African, Southern European, Kurdish Jewish, Middle Eastern, Central Asian, South Asian descentHereditary Amyloidosis (TTR-Related)Genetic risk for a form of nerve and heart damage3 variants in the TTR gene; relevant for African American, West African, Portuguese, Northern Swedish, Japanese, Irish, British descentHereditary Hemochromatosis (HFE‑Related)Genetic risk for iron overload2 variants in the HFE gene; relevant for European descentHereditary ThrombophiliaGenetic risk for harmful blood clots2 variants in the F2 and F5 genes; relevant for European descentLate-Onset Alzheimer's DiseaseGenetic risk for a form of dementia1 variant in the APOE gene; variant found and studied in many ethnicitiesMUTYH-Associated PolyposisGenetic risk for a specific colorectal cancer syndrome2 variants in the MUTYH gene; relevant for Northern European descentParkinson's DiseaseGenetic risk for a formof movement impairment2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descentSee sample report- Health PredispositionWellness Reports5+ reportsAlcohol Flush ReactionCaffeine ConsumptionDeep SleepGenetic WeightLactose IntoleranceMuscle CompositionSaturated Fat and WeightSleep MovementSee sample report- WellnessCarrier Status Reports*40+ reportsARSACS1 variant in the SACS gene; relevant for French Canadian descentAgenesis of the Corpus Callosum with Peripheral Neuropathy1 variant in the SLC12A6 gene; relevant for French Canadian descentAutosomal Recessive Polycystic Kidney Disease3 variants in the PKHD1 geneBeta Thalassemia and Related Hemoglobinopathies10 variants in the HBB gene; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descentBloom Syndrome1 variant in the BLM gene; relevant for Ashkenazi Jewish descentCanavan Disease3 variants in the ASPA gene; relevant for Ashkenazi Jewish descentCongenital Disorder of Glycosylation Type 1a (PMM2-CDG)2 variants in the PMM2 gene; relevant for Ashkenazi Jewish, Danish descentCystic Fibrosis29 variants in the CFTR gene; relevant for Ashkenazi Jewish, European, Hispanic/Latino descentD-Bifunctional Protein Deficiency2 variants in the HSD17B4 geneDihydrolipoamide Dehydrogenase Deficiency1 variant in the DLD gene; relevant for Ashkenazi Jewish descentFamilial Dysautonomia1 variant in the ELP1 gene; relevant for Ashkenazi Jewish descentFamilial Hyperinsulinism (ABCC8-Related)3 variants in the ABCC8 gene; relevant for Ashkenazi Jewish descentFamilial Mediterranean Fever7 variants in the MEFV gene; relevant for Arab, Armenian, Sephardic Jewish, Turkish descentFanconi Anemia Group C3 variants in the FANCC gene; relevant for Ashkenazi Jewish descentGRACILE Syndrome1 variant in the BCS1L gene; relevant for Finnish descentGaucher Disease Type 13 variants in the GBA gene; relevant for Ashkenazi Jewish descentGlycogen Storage Disease Type Ia1 variant in the G6PC gene; relevant for Ashkenazi Jewish descentGlycogen Storage Disease Type Ib2 variants in the SLC37A4 geneHereditary Fructose Intolerance4 variants in the ALDOB gene; relevant for European descentHerlitz Junctional Epidermolysis Bullosa (LAMB3-Related)3 variants in the LAMB3 geneLeigh Syndrome, French Canadian Type1 variant in the LRPPRC gene; relevant for French Canadian descentLimb-Girdle Muscular Dystrophy Type 2D1 variant in the SGCA geneLimb-Girdle Muscular Dystrophy Type 2E1 variant in the SGCB gene; relevant for Amish descentLimb-Girdle Muscular Dystrophy Type 2I1 variant in the FKRP geneMCAD Deficiency4 variants in the ACADM gene; relevant for European descentMaple Syrup Urine Disease Type 1B2 variants in the BCKDHB gene; relevant for Ashkenazi Jewish descentMucolipidosis Type IV1 variant in the MCOLN1 gene; relevant for Ashkenazi Jewish descentNeuronal Ceroid Lipofuscinosis (CLN5-Related)1 variant in the CLN5 gene; relevant for Finnish descentNeuronal Ceroid Lipofuscinosis (PPT1-Related)3 variants in the PPT1 gene; relevant for Finnish descentNiemann-Pick Disease Type A3 variants in the SMPD1 gene; relevant for Ashkenazi Jewish descentNijmegen Breakage Syndrome1 variant in the NBN geneNonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)2 variants in the GJB2 gene; relevant for Ashkenazi Jewish, European descentPendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related)6 variants in the SLC26A4 genePhenylketonuria and Related Disorders23 variants in the PAH gene; relevant for Irish, Northern European descentPrimary Hyperoxaluria Type 21 variant in the GRHPR genePyruvate Kinase Deficiency1 variant in the PKLR geneRhizomelic Chondrodysplasia Punctata Type 11 variant in the PEX7 geneSalla Disease1 variant in the SLC17A5 gene; relevant for Finnish, Swedish descentSickle Cell Anemia1 variant in the HBB gene; relevant for African American, African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descentSjögren-Larsson Syndrome1 variant in the ALDH3A2 gene; relevant for Swedish descentTay-Sachs Disease4 variants in the HEXA gene; relevant for Ashkenazi Jewish, Cajun descentTyrosinemia Type I4 variants in the FAH gene; relevant for French Canadian, Finnish descentUsher Syndrome Type 1F1 variant in the PCDH15 gene; relevant for Ashkenazi Jewish descentUsher Syndrome Type 3A1 variant in the CLRN1 gene; relevant for Ashkenazi Jewish descentZellweger Syndrome Spectrum (PEX1-Related)1 variant in the PEX1 geneSee sample report- Carrier StatusReports included in 23andMe+:Pharmacogenetics Reports**CYP2C19 Drug MetabolismDNA variants that influence how the body processes certain medications for depression, acid reflux, heart disease and other conditionsDPYD Drug MetabolismDNA variants that influence how the body processes certain cancer medicationsSLCO1B1 Drug TransportA DNA variant that influences how the body processes certain medicationsHealth Predisposition Reports*5+ reportsAtrial Fibrillation ( Powered by 23andMe Research )Genetic likelihood for a type of irregular heartbeatCoronary Artery Disease ( Powered by 23andMe Research )Genetic likelihood for a type of heart diseaseGout ( Powered by 23andMe Research )Genetic likelihood for condition where one or more joints suddenly becomes painful and swollenHigh Blood Pressure ( Powered by 23andMe Research )Genetic likelihood of developing high blood pressureKidney Stones ( Powered by 23andMe Research )Genetic likelihood for solid, pebble-like masses that form in the kidneysLDL Cholesterol ( Powered by 23andMe Research )Genetic likelihood of developing high levels of LDL ("bad") cholesterolMigraine ( Powered by 23andMe Research )Genetic likelihood of experiencing migraine headachesNonalcoholic Fatty Liver Disease ( Powered by 23andMe Research )Genetic likelihood for a condition where fat builds up in the liverObstructive Sleep Apnea ( Powered by 23andMe Research )Genetic likelihood for a condition where breathing stops and starts repeatedly during sleepPolycystic Ovary Syndrome (PCOS)( Powered by 23andMe Research; available for females only )Genetic likelihood for a hormone disorder that affects femalesRestless Legs Syndrome ( Powered by 23andMe Research )Genetic likelihood for a condition characterized by an uncontrollable urge to move one's legsTriglycerides ( Powered by 23andMe Research )Genetic likelihood of developing high levels of triglycerides (a type of lipid)Uterine Fibroids( Powered by 23andMe Research; available for females only )Genetic likelihood for a common type of non-cancerous growth in the uterusWellness ReportsCat AllergyDog Allergy

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End Time: 2024-10-31T17:12:46.000Z

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