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rs81002836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs81002836(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362521
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002836
ebirs81002836
HLIrs81002836
Exacrs81002836
Varsomers81002836
Maprs81002836
PheGenIrs81002836
hapmaprs81002836
1000 genomesrs81002836
hgdprs81002836
ensemblrs81002836
gopubmedrs81002836
geneviewrs81002836
scholarrs81002836
googlers81002836
pharmgkbrs81002836
gwascentralrs81002836
openSNPrs81002836
23andMers81002836
23andMe allrs81002836
SNP Nexus

SNPshotrs81002836
SNPdbers81002836
MSV3drs81002836
GWAS Ctlgrs81002836
Max Magnitude6
ClinVar
Risk rs81002836(G;G)
Alt rs81002836(G;G)
Reference rs81002836(A;A)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32936658A>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045321.3, RCV000077414.4, RCV000131088.2,