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rs81002886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002886(A;G)
Make rs81002886(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376668
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002886
ebirs81002886
HLIrs81002886
Exacrs81002886
Varsomers81002886
Maprs81002886
PheGenIrs81002886
hapmaprs81002886
1000 genomesrs81002886
hgdprs81002886
ensemblrs81002886
gopubmedrs81002886
geneviewrs81002886
scholarrs81002886
googlers81002886
pharmgkbrs81002886
gwascentralrs81002886
openSNPrs81002886
23andMers81002886
23andMe allrs81002886
SNP Nexus

SNPshotrs81002886
SNPdbers81002886
MSV3drs81002886
GWAS Ctlgrs81002886
Max Magnitude0
ClinVar
Risk rs81002886(G,T;G,T)
Alt rs81002886(G,T;G,T)
Reference rs81002886(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32950805A>G; NC_000013.10:g.32950805A>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031755.4, RCV000045583.2, RCV000045584.2,