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ClinVar/Reports

From SNPedia


Name Significance Disease Normal S M R Risk S M R
Rs1008642 255 Distal myopathy, Tateyama type not provided not specified Cardiovascular phenotype Limb-Girdle Muscular Dystrophy, Dominant Romano-Ward syndrome Hypertrophic cardiomyopathy Caveolinopathy Long QT syndrome Rs1008642(C;C) common in clinvar 0 Good Rs1008642(G;G) Rs1008642(T;T)
Rs1021737 255 Homocysteine, total plasma, elevated Cystathioninuria Rs1021737(G;G) common in clinvar 0 Good Rs1021737(T;T) significantly higher plasma total homocysteine concentration 3 Bad
Rs1024611 255 Spina bifida, susceptibility to Coronary artery disease, modifier of Coronary artery disease, development of, in hiv Mycobacterium tuberculosis, susceptibility to Rs1024611(T;T) normal risk 0 Good Rs1024611(C;C) increased risk of exercise induced ischemia, Increased CCL2 levels; increased rate of HIV progression 2.2 Bad
Rs10262966 255 Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Rs10262966(A;A) common in clinvar 0 Good Rs10262966(G;G)
Rs1041981 255 Myocardial infarction Rs1041981(C;C) normal Rs1041981(A;A) Higher myocardial infarction risk 2 Bad
Rs1042031 255 not specified Familial hypercholesterolemia Familial hypobetalipoproteinemia Rs1042031(G;G) common in clinvar 0 Good Rs1042031(A;A) Rs1042031(T;T)
Rs1042034 255 not specified Familial hypercholesterolemia Familial hypobetalipoproteinemia Rs1042034(G;G) common in clinvar 0 Good Rs1042034(A;A)
Rs1042077 255 not specified Cystic fibrosis Rs1042077(T;T) common/normal 0 Good Rs1042077(A;A) Rs1042077(G;G)
Rs1042395 255 not specified Glycogen storage disease, type II Rs1042395(G;G) common in clinvar 0 Good Rs1042395(A;A)
... further results


Name Significance Disease Normal S M R Risk S M R
Rs1006246556 5 Primary pulmonary hypertension Rs1006246556(G;G) Rs1006246556(A;A)
Rs10065172 5 Inflammatory bowel disease 19 Rs10065172(C;C) common in complete genomics 0 Good Rs10065172(T;T)
Rs1010078101 5 not provided Rs1010078101(G;G) Rs1010078101(A;A)
Rs10127939 5 Immunodeficiency 20 not specified Rs10127939(T;T) common in clinvar 0 Good Rs10127939(A;A) Rs10127939(G;G)
Rs1013079991 5 Congenital generalized lipodystrophy type 2 Rs1013079991(T;T) Rs1013079991(C;C)
Rs10151259 5 Cone-rod dystrophy 13 not provided not specified Leber congenital amaurosis Cone-Rod Dystrophy, Recessive Rs10151259(G;G) common in clinvar 0 Good Rs10151259(T;T) Recessive genotype uncertain pathogenicity 2 Bad
Rs1019221239 5 Hereditary cancer-predisposing syndrome Rs1019221239(T;T) Rs1019221239(C;C)
Rs1020621286 5 not provided Rs1020621286(T;T) Rs1020621286(G;G)
Rs10250779 5 Glycogen storage disease type X not provided Rs10250779(G;G) common in clinvar 0 Good Rs10250779(A;A) Rs10250779(C;C)
... further results


Name Significance Disease Normal S M R Risk S M R
Rs1001916923 4 not provided Rs1001916923(A;A) Rs1001916923(G;G) Rs1001916923(T;T)
Rs1002820022 4 not provided Rs1002820022(G;G) Rs1002820022(A;A) Rs1002820022(T;T)
Rs1004428835 4 not provided Rs1004428835(C;C) Rs1004428835(T;T)
Rs1005670966 4 not provided Rs1005670966(G;G) Rs1005670966(A;A)
Rs1005731602 4 not provided Rs1005731602(C;C) Rs1005731602(T;T)
Rs1006150317 4 Glutaric aciduria, type 1 Rs1006150317(G;G) Rs1006150317(T;T)
Rs1008240677 4 Ataxia with vitamin E deficiency Rs1008240677(G;G) Rs1008240677(A;A)
Rs1012472070 4 not provided Rs1012472070(G;G) Rs1012472070(A;A) Rs1012472070(T;T)
Rs1017182331 4 not provided Rs1017182331(G;G) Rs1017182331(A;A)
... further results


Name Significance Disease Normal S M R Risk S M R
Rs1049650 7 Rs1049650(G;G) common in clinvar 0 Good Rs1049650(C;C)
Rs1049663 7 Rs1049663(G;G) common in clinvar 0 Good Rs1049663(T;T)
Rs1049668 7 Rs1049668(G;G) common in clinvar 0 Good Rs1049668(A;A)
Rs1049709 7 Rs1049709(A;A) common in clinvar 0 Good Rs1049709(G;G)
Rs1049724 7 Rs1049724(G;G) common in clinvar 0 Good Rs1049724(A;A)
Rs1049853 7 Rs1049853(C;C) common in clinvar 0 Good Rs1049853(T;T)
Rs1050105 7 Rs1050105(C;C) common in clinvar 0 Good Rs1050105(T;T)
Rs1050106 7 Rs1050106(C;C) common in clinvar 0 Good Rs1050106(T;T)
Rs1050118 7 Rs1050118(G;G) common in clinvar 0 Good Rs1050118(A;A)
... further results


Name Significance Disease Normal S M R Risk S M R
Rs10019009 2 Hypophosphatemic Rickets, Recessive Rs10019009(A;A) Rs10019009(G;G) Rs10019009(T;T)
Rs1002076 2 Charcot-Marie-Tooth, Type 2 Neuroblastoma Pheochromocytoma Rs1002076(C;C) Rs1002076(T;T)
Rs1003723 2 Familial hypercholesterolemia Rs1003723(C;C) common in clinvar 0 Good Rs1003723(T;T)
Rs10046 2 Aromatase deficiency Rs10046(C;C) Rs10046(T;T)
Rs10079250 2 Hereditary diffuse leukoencephalopathy with spheroids Rs10079250(T;T) Rs10079250(C;C)
Rs10087163 2 not specified Rs10087163(A;A) common in clinvar 0 Good Rs10087163(G;G) common on affy axiom data 0 Good
Rs10103355 2 not specified Farber's lipogranulomatosis Rs10103355(A;A) Rs10103355(G;G) common in complete genomics 0 Good
Rs1012729 2 not specified Hereditary sensory and autonomic neuropathy type II Pseudohypoaldosteronism, type 2 Rs1012729(G;G) altered pediatric blood pressure Rs1012729(A;A) Rs1012729(C;C) Rs1012729(T;T)
Rs1014867 2 not specified Rs1014867(C;C) Rs1014867(T;T)
... further results



Name Significance Disease Normal S M R Risk S M R
Rs104893623 1 Irido-corneo-trabecular dysgenesis Rs104893623(G;G) common in clinvar 0 Good Rs104893623(A;A)
Rs104893752 1 Dominant hereditary optic atrophy Rs104893752(C;C) common in clinvar 0 Good Rs104893752(T;T)
Rs104894599 1 Mucopolysaccharidosis, MPS-III-B Rs104894599(C;C) common in clinvar 0 Good Rs104894599(A;A)
Rs104894600 1 Mucopolysaccharidosis, MPS-III-B Rs104894600(T;T) common in clinvar 0 Good Rs104894600(C;C)
Rs104894776 1 Immunodeficiency with hyper IgM type 1 Rs104894776(G;G) common in clinvar 0 Good Rs104894776(A;A)
Rs104894807 1 Rs104894807(T;T) common in clinvar 0 Good Rs104894807(C;C)
Rs104894893 1 Congenital adrenal hypoplasia, X-linked Rs104894893(G;G) common in clinvar 0 Good Rs104894893(A;A)
Rs104895089 1 Familial Mediterranean fever Rs104895089(A;A) common in clinvar 0 Good Rs104895089(C;C) Rs104895089(G;G)
Rs104895103 1 Familial Mediterranean fever not specified Rs104895103(A;A) common in clinvar 0 Good Rs104895103(C;C) Rs104895103(G;G)
... further results



Name Significance Disease Normal S M R Risk S M R
Rs10131 3 Lig4 syndrome Severe combined immunodeficiency with sensitivity to ionizing radiation Rs10131(G;G) Rs10131(A;A)
Rs10183087 3 Common Variable Immune Deficiency, Recessive not specified Rs10183087(A;A) Rs10183087(C;C) Rs10183087(G;G)
Rs10234329 3 Cystic fibrosis Rs10234329(A;A) common in complete genomics 0 Good Rs10234329(C;C)
Rs10246939 6 Phenylthiocarbamide tasting Rs10246939(T;T) possibly unable to taste bitterness 1.1 Rs10246939(C;C) can taste bitter 0.1
Rs10306114 6 aspirin response - Efficacy Rs10306114(A;A) normal 0 Good Rs10306114(G;G) Higher risk of bleeding during coronary angiography 3 Bad
Rs1034762 3 not specified Stickler Syndrome, Dominant Type II Collagenopathies Rs1034762(T;T) Rs1034762(G;G) 0
Rs1038426 3 Isolated GnRH Deficiency Rs1038426(C;C) Rs1038426(A;A) Rs1038426(T;T)
Rs1040461 3 Carpenter syndrome Rs1040461(C;C) common in complete genomics 0 Good Rs1040461(T;T)
Rs1041983 6 ethambutol, isoniazid, pyrazinamide, and rifampin response - Toxicity/ADR Rs1041983(C;C) 0 Rs1041983(T;T)
Rs1042173 3 Behavior disorder Rs1042173(T;T) among alcoholics, likely to be heavier drinkers Bad Rs1042173(G;G) normal
Rs1042522 6 not specified not provided Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1 CODON 72 POLYMORPHISM, (rs1042522) paclitaxel response - Efficacy, Toxicity/ADR cyclophosphamide response - Efficacy, Toxicity/ADR antineoplastic agents response - Efficacy, Toxicity/ADR fluorouracil response - Efficacy, Toxicity/ADR cisplatin response - Efficacy, Toxicity/ADR Li-Fraumeni syndrome Rs1042522(C;C) Live 3 years longer. Chemotherapy is more effective. 3 Good Rs1042522(G;G) Rs1042522(A;A)
Rs1042571 3 Monogenic Non-Syndromic Obesity Proopiomelanocortin deficiency Rs1042571(C;C) Rs1042571(T;T)
Rs1043424 3 Congenital disorder of glycosylation Parkinson Disease, Recessive Rs1043424(A;A) 0 Rs1043424(C;C)
Rs1043953 3 Cardiomyopathy, ARVC Xeroderma pigmentosum Rs1043953(A;A) Rs1043953(G;G)
Rs10455872 6 HMG CoA reductase inhibitors response - Efficacy Rs10455872(A;A) common/normal 0 Good Rs10455872(G;G) 2,57x increased Coronary Heart disease risk 3 Bad
Rs1045642 6 ondansetron response - Efficacy oxycodone response - Dosage methadone response - Dosage methotrexate response - Toxicity/ADR nevirapine response - Toxicity/ADR tramadol response - Dosage morphine response - Dosage digoxin response - Other opioids response - Dosage fentanyl response - Dosage MDR1 POLYMORPHISM Non-small cell lung cancer Rs1045642(T;T) altered drug metabolism and bioavailability; moderately increased risk for certain cancers 3 Bad Rs1045642(C;C) Rs1045642(A;A)
Rs1046276 3 Dilated Cardiomyopathy, Dominant Rs1046276(T;T) Rs1046276(C;C)
Rs1048108 3 Hereditary cancer-predisposing syndrome not specified Neoplasm of breast Rs1048108(C;C) common in clinvar 0 Good Rs1048108(T;T)
Rs104894184 3 Hereditary cancer-predisposing syndrome Rs104894184(T;T) common in complete genomics 0 Good Rs104894184(A;A) Rs104894184(C;C) Rs104894184(G;G)
Rs104894840 6 Fabry disease Deoxygalactonojirimycin response not provided Rs104894840(G;G) common in clinvar 0 Good Rs104894840(A;A) Rs104894840(C;C)
Rs104894955 3 not provided Non-syndromic X-linked intellectual disability Rs104894955(C;C) common in clinvar 0 Good Rs104894955(T;T)
Rs104895431 3 Sarcoidosis, early-onset Crohn disease Rs104895431(C;C) Rs104895431(T;T)
Rs104895444 3 Sarcoidosis, early-onset Crohn disease Rs104895444(G;G) Rs104895444(A;A)
Rs10490923 3 Macular degeneration Rs10490923(G;G) common in complete genomics 0 Good Rs10490923(A;A)
Rs1049331 3 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Macular degeneration Rs1049331(C;C) common in clinvar 0 Good Rs1049331(T;T)
Rs1049434 3 not specified Hyperinsulinism, Dominant Rs1049434(T;T) common in clinvar 0 Good Rs1049434(A;A)
Rs10497203 6 radiotherapy response - Toxicity/ADR Rs10497203(A;A) common in clinvar 0 Good Rs10497203(C;C)
Rs1050171 3 not specified Lung cancer Rs1050171(G;G) common in clinvar 0 Good Rs1050171(A;A)
Rs1050239 3 not specified Sphingomyelin/cholesterol lipidosis Rs1050239(G;G) common in clinvar 0 Good Rs1050239(A;A) Rs1050239(C;C)
Rs1050757 3 Glucose 6 phosphate dehydrogenase deficiency Rs1050757(A;A) common/normal 0 Good Rs1050757(G;G) likely benign (ClinVar) 0 Good
Rs1050783 3 Factor xiii, a subunit, deficiency of Rs1050783(G;G) Rs1050783(A;A)
Rs10509681 6 rosiglitazone response - Dosage Rs10509681(T;T) common on affy axiom data 0 Good Rs10509681(C;C) 2
Rs1052030 3 not specified not provided Nonsyndromic Hearing Loss, Dominant Retinitis pigmentosa-deafness syndrome Nonsyndromic Hearing Loss, Recessive Rs1052030(T;T) common in clinvar 0 Good Rs1052030(A;A) Rs1052030(C;C)
Rs1056468 3 Familial atrial fibrillation Rs1056468(A;A) Rs1056468(T;T)
Rs1056836 6 not specified paclitaxel response - Efficacy docetaxel response - Efficacy Rs1056836(G;G) 0.3x decreased risk for prostate cancer 2 Good Rs1056836(C;C) normal
Rs1056892 6 anthracyclines and related substances response - Toxicity/ADR Rs1056892(G;G) common in clinvar 0 Good Rs1056892(A;A)
Rs1057091 3 Primary autosomal recessive microcephaly 1 not specified Primary Microcephaly, Recessive Rs1057091(C;C) common in clinvar 0 Good Rs1057091(T;T)
Rs1057868 3 not specified Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Rs1057868(C;C) normal Rs1057868(T;T) 1.6x higher overall CYP3A activity 1.6
Rs1059611 3 Hyperlipoproteinemia, type I Rs1059611(T;T) Rs1059611(C;C)
Rs1061237 3 Osteogenesis Imperfecta, Dominant Ehlers-Danlos syndrome, type 7A Infantile cortical hyperostosis Rs1061237(T;T) Rs1061237(A;A) Rs1061237(C;C)
Rs1062087 3 not specified Rs1062087(G;G) common in clinvar 0 Good Rs1062087(A;A)
Rs1063856 3 not specified not provided von Willebrand disorder Rs1063856(A;A) common in clinvar 0 Good Rs1063856(C;C) Rs1063856(G;G)
Rs1063857 3 not specified von Willebrand disorder Rs1063857(T;T) Rs1063857(C;C)
Rs1064074 3 not specified Nonsyndromic Hearing Loss, Recessive Retinitis pigmentosa-deafness syndrome Rs1064074(G;G) common in clinvar 0 Good Rs1064074(C;C) Rs1064074(T;T)
Rs1065852 6 Debrisoquine, poor metabolism of Rs1065852(C;C) normal 0 Good Rs1065852(T;T) Homozygous for CYP2D6 decreased or non-functioning variants. 3.2 Bad
Rs1071646 3 not provided not specified Cardiovascular phenotype Dilated Cardiomyopathy, Dominant Hypertrophic cardiomyopathy Rs1071646(C;C) common in clinvar 0 Good Rs1071646(A;A)
Rs10754602 3 not specified Cardiomyopathy, ARVC Catecholaminergic polymorphic ventricular tachycardia Rs10754602(T;T) common in clinvar 0 Good Rs10754602(A;A) Rs10754602(C;C)
Rs1076560 6 cocaine response - Toxicity/ADR Rs1076560(C;C) normal 0 Rs1076560(A;A) influences working memory 2
Rs10824792 3 Mannose-binding protein deficiency Rs10824792(C;C) Rs10824792(T;T)
... further results


 ClinVar CLNSIGClinVar CLNDBNRefGenoRiskGenoGMAFOn microarray
rs6262630552-methyl-3-hydroxybutyric aciduriars62626305(G;G)Rs62626305(C;C)23andMe v3
23andMe v4
Ancestry v2
rs2893547552-methyl-3-hydroxybutyric aciduriars28935475(C;C)Rs28935475(T;T)23andMe v1
Illumina Human 1M
23andMe v2
23andMe v3
23andMe v4
rs2893547652-methyl-3-hydroxybutyric aciduriars28935476(C;C)Rs28935476(G;G)23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs6445521-hydroxylase deficiencyrs6445(C;C)rs6445(T;T)23andMe v4
rs64675not specified
21-hydroxylase deficiency
rs6467(G;G)Rs6467(C;C)
rs6467(T;T)
0.336FTDNA2
HumanOmni1Quad
Illumina Human 1M
rs12530380521-hydroxylase deficiencyrs12530380(T;T)rs12530380(A;A)23andMe v3
23andMe v4
rs2893488053 beta-Hydroxysteroid dehydrogenase deficiencyrs28934880(C;C)rs28934880(A;A)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs2893789953-Methylglutaconic aciduria type 3rs28937899(C;C)Rs28937899(T;T)23andMe v3
23andMe v4
rs93329645Micropenis
not provided
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
rs9332964(G;G)rs9332964(A;A)9.183e-423andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs115451054-Alpha-hydroxyphenylpyruvate hydroxylase deficiencyrs1154510(A;A)rs1154510(G;G)0.13223andMe v1
23andMe v2
23andMe v3
23andMe v4
FTDNA2
FamilyTreeDNA
HumanOmni1Quad
Illumina Human 1M
Ancestry v2
rs283745445Tetralogy of Fallot
46,XY sex reversal 9
rs28374544(A;A)Rs28374544(G;G)0.033123andMe v1
Illumina Human 1M
23andMe v2
23andMe v3
23andMe v4
rs725527785Cholecystitis
Cholestasis, intrahepatic, of pregnancy 3
Progressive familial intrahepatic cholestasis 3
ABCB4-Related Intrahepatic Cholestasis
rs72552778(C;C)Rs72552778(T;T)23andMe v3
23andMe v4
Ancestry v2
rs127215105ACTH deficiencyrs12721510(C;C)rs12721510(A;A)0.020223andMe v3
FTDNA2
HumanOmni1Quad
Illumina Human 1M
23andMe v4
Ancestry v2
rs289408925ACTH resistancers28940892(A;A)Rs28940892(G;G)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs626370145Leber congenital amaurosis 4
not provided
AIPL1-Related Disorders
rs62637014(G;G)Rs62637014(A;A)023andMe v3
23andMe v4
Ancestry v2
rs5536685ALPHA-2A ADRENERGIC RECEPTOR, OVEREXPRESSION or TYPE 2 DIABETES SUSCEPTIBILITY (safer to say the former than the latter)rs553668(T;T)rs553668(C;C)0.2923andMe v1
23andMe v2
23andMe v3
FTDNA2
HumanOmni1Quad
Illumina Human 1M
23andMe v4
Ancestry v2
rs18004355AMINOLEVULINATE DEHYDRATASE, ALAD*1/ALAD*2 POLYMORPHISM
Porphobilinogen synthase deficiency
rs1800435(G;G)Rs1800435(C;C)0.046823andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs174735ANTICHYMOTRYPSIN BONN 1
not specified
rs17473(C;C)Rs17473(G;G)
Rs17473(T;T)
0.0018423andMe v1
23andMe v3
Affy GenomeWide 6
HumanOmni1Quad
23andMe v4
Ancestry v2
rs289315785APOE2 VARIANTrs28931578(G;G)Rs28931578(A;A)
Rs28931578(C;C)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs289315775APOE3 VARIANTrs28931577(G;G)Rs28931577(A;A)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289315765APOE3(-)-FREIBURGrs28931576(A;A)Rs28931576(G;G)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289315795APOE4(+)rs28931579(A;A)Rs28931579(C;C)23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs7694525APOE4(-)-FREIBURG
not specified
rs769452(T;T)Rs769452(C;C)0.0013823andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289294765APOLIPOPROTEIN A-I (BALTIMORE)rs28929476(G;G)Rs28929476(T;T)23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289315735APOLIPOPROTEIN A-I (MILANO)rs28931573(C;C)rs28931573(T;T)23andMe v2
23andMe v3
23andMe v4
rs51105APOLIPOPROTEIN A-IV POLYMORPHISM, APOA4*1/APOA4*2rs5110(G;G)Rs5110(T;T)0.033123andMe v2
23andMe v3
FTDNA2
HumanOmni1Quad
Illumina Human 1M
23andMe v4
Ancestry v2
rs51225APOLIPOPROTEIN C-II (SAN FRANCISCO)rs5122(G;G)Rs5122(A;A)0.00184Illumina Human 1M
Ancestry v2
rs289991135APRT deficiency, Japanese type
Adenine phosphoribosyltransferase deficiency
rs28999113(T;T)Rs28999113(C;C)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289354975Aarskog syndrome
not provided
rs28935497(G;G)Rs28935497(A;A)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289402825Acampomelic campomelic dysplasiars28940282(C;C)Rs28940282(T;T)23andMe v2
23andMe v3
23andMe v4
rs289316145Achondroplasia
Epidermal nevus
not provided
rs28931614(G;G)Rs28931614(A;A)
Rs28931614(C;C)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs289330685Hypochondroplasia
Thanatophoric dysplasia type 1
not provided
Achondroplasia
Short stature
rs28933068(C;C)Rs28933068(A;A)
Rs28933068(G;G)
Rs28933068(T;T)
23andMe v2
23andMe v3
23andMe v4
rs289378895Acroerythrokeratodermars28937889(A;A)Rs28937889(C;C)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289294795Acromesomelic dysplasia Maroteaux typers28929479(T;T)Rs28929479(A;A)23andMe v1
23andMe v3
23andMe v4
Ancestry v2
rs289315815Acromesomelic dysplasia Maroteaux typers28931581(C;C)Rs28931581(A;A)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289315825Acromesomelic dysplasia Maroteaux typers28931582(T;T)Rs28931582(G;G)23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289315905Acute myeloid leukemiars28931590(A;A)rs28931590(T;T)23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs289334065Thyroid cancer, follicular
Spermatocytic seminoma
Chronic lymphocytic leukemia
Malignant melanoma of skin
Pancreatic adenocarcinoma
Neoplasm of the thyroid gland
Hepatocellular carcinoma
Adenocarcinoma of stomach
Squamous cell carcinoma of lung
Transitional cell carcinoma of the bladder
Acute myeloid leukemia
Colorectal Neoplasms
Malignant neoplasm of body of uterus
Multiple myeloma
Adenocarcinoma of lung
Neoplasm of breast
rs28933406(C;C)Rs28933406(A;A)
rs28933406(G;G)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs115542905Acute myeloid leukemia
Adenocarcinoma of lung
Adenocarcinoma of stomach
Adrenocortical carcinoma
Chronic lymphocytic leukemia
Colorectal Neoplasms
Epidermal nevus
Epidermal nevus syndrome
Giant pigmented hairy nevus
Glioblastoma
Hepatocellular carcinoma
Malignant melanoma
Malignant melanoma of skin
Malignant neoplasm of body of uterus
Multiple myeloma
Nasopharyngeal Neoplasms
Neoplasm of brain
Neoplasm of the thyroid gland
Neurocutaneous melanosis
Non-small cell lung cancer
Ovarian Serous Cystadenocarcinoma
Renal cell carcinoma
Thyroid cancer, follicular
Transitional cell carcinoma of the bladder
not provided
rs11554290(A;A)Rs11554290(C;C)
Rs11554290(G;G)
rs11554290(T;T)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs289345765Li-Fraumeni syndrome 1
Thyroid cancer, anaplastic
Hereditary cancer-predisposing syndrome
not provided
Pancreatic adenocarcinoma
Neoplasm of brain
Squamous cell carcinoma of the head and neck
Chronic lymphocytic leukemia
Colorectal Neoplasms
Adenocarcinoma of lung
Medulloblastoma
Adrenocortical carcinoma
Malignant melanoma of skin
Brainstem glioma
Malignant neoplasm of body of uterus
Adenocarcinoma of prostate
Acute myeloid leukemia
Oesophageal carcinoma
Hepatocellular carcinoma
Small cell lung cancer
Multiple myeloma
Adenocarcinoma of stomach
Neoplasm of breast
Uterine Carcinosarcoma
Squamous cell carcinoma of lung
Ovarian Serous Cystadenocarcinoma
Transitional cell carcinoma of the bladder
Glioblastoma
Neoplasm
Li-Fraumeni syndrome
rs28934576(G;G)rs28934576(A;A)
Rs28934576(C;C)
Rs28934576(T;T)
4.591e-423andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs10646515Gaucher disease type 3C
Gaucher's disease, type 1
Acute neuronopathic Gaucher's disease
Subacute neuronopathic Gaucher's disease
Gaucher disease, perinatal lethal
Gaucher disease
not provided
rs1064651(G;G)rs1064651(C;C)23andMe v1
23andMe v3
23andMe v4
Ancestry v2
rs289345755Li-Fraumeni syndrome 1
Hereditary cancer-predisposing syndrome
Li-Fraumeni-like syndrome
Adenocarcinoma
Li-Fraumeni syndrome
not provided
Uterine Carcinosarcoma
Adenocarcinoma of lung
Neoplasm of breast
Ovarian Serous Cystadenocarcinoma
Adenocarcinoma of stomach
Glioblastoma
Transitional cell carcinoma of the bladder
Pancreatic adenocarcinoma
Adenocarcinoma of prostate
Brainstem glioma
Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of lung
Oesophageal carcinoma
Neoplasm of brain
Hepatocellular carcinoma
Colorectal Neoplasms
Neoplasm
rs28934575(G;G)Rs28934575(A;A)
Rs28934575(T;T)
rs28934575(C;C)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs289315895Pilomatrixoma
Hepatoblastoma
Malignant tumor of prostate
Squamous cell carcinoma of the head and neck
Adenocarcinoma of stomach
Ovarian Neoplasms
Adrenocortical carcinoma
Malignant neoplasm of body of uterus
Malignant melanoma of skin
Adenocarcinoma of lung
Hepatocellular carcinoma
Medulloblastoma
Craniopharyngioma
Malignant melanoma
rs28931589(G;G)Rs28931589(A;A)
Rs28931589(T;T)
Rs28931589(C;C)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs115542735Somatotroph adenoma
Polyostotic fibrous dysplasia, somatic, mosaic
Cushing's syndrome
McCune-Albright syndrome
Sex cord-stromal tumor
Neoplasm
Squamous cell carcinoma of the head and neck
Hepatocellular carcinoma
Colorectal Neoplasms
Pancreatic adenocarcinoma
Adenocarcinoma of lung
Uterine cervical neoplasms
Neoplasm of breast
Adrenocortical carcinoma
Adenocarcinoma of stomach
Malignant melanoma of skin
rs11554273(C;C)Rs11554273(A;A)
Rs11554273(G;G)
Rs11554273(T;T)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
rs289345735Hepatoblastoma
Osteosarcoma
Hereditary cancer-predisposing syndrome
Li-Fraumeni syndrome
not provided
Squamous cell carcinoma of the skin
Malignant lymphoma, non-Hodgkin
Brainstem glioma
Oesophageal carcinoma
Neoplasm of breast
Squamous cell carcinoma of the head and neck
Uterine Carcinosarcoma
Adenocarcinoma of lung
Malignant melanoma of skin
Papillary renal cell carcinoma, sporadic
Neoplasm of brain
Glioblastoma
Malignant neoplasm of body of uterus
Transitional cell carcinoma of the bladder
Colorectal Neoplasms
Pancreatic adenocarcinoma
Ovarian Serous Cystadenocarcinoma
Carcinoma of gallbladder
Renal cell carcinoma
rs28934573(C;C)rs28934573(G;G)
Rs28934573(T;T)
Rs28934573(A;A)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
Ancestry v2
rs289315885Hepatoblastoma
Pilomatrixoma
Adenocarcinoma of prostate
Transitional cell carcinoma of the bladder
Medulloblastoma
Malignant neoplasm of body of uterus
Adenocarcinoma of stomach
Malignant melanoma of skin
Hepatocellular carcinoma
Esophageal Squamous Cell Carcinoma
Endometrial neoplasm
Uterine cervical neoplasms
Malignant melanoma
Craniopharyngioma
rs28931588(G;G)Rs28931588(A;A)
Rs28931588(C;C)
Rs28931588(T;T)
23andMe v1
23andMe v2
23andMe v3
23andMe v4
... further results