Have questions? Visit https://www.reddit.com/r/SNPedia

rs81002831

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002831(C;C)
Make rs81002831(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32330918
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002831
ebirs81002831
HLIrs81002831
Exacrs81002831
Varsomers81002831
Maprs81002831
PheGenIrs81002831
hapmaprs81002831
1000 genomesrs81002831
hgdprs81002831
ensemblrs81002831
gopubmedrs81002831
geneviewrs81002831
scholarrs81002831
googlers81002831
pharmgkbrs81002831
gwascentralrs81002831
openSNPrs81002831
23andMers81002831
23andMe allrs81002831
SNP Nexus

SNPshotrs81002831
SNPdbers81002831
MSV3drs81002831
GWAS Ctlgrs81002831
Max Magnitude0
ClinVar
Risk rs81002831(C;C)
Alt rs81002831(C;C)
Reference rs81002831(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32905055G>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045063.2, RCV000114011.1, RCV000215277.1,