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

rs81002844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs81002844(C;G)
Make rs81002844(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379747
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002844
ebirs81002844
HLIrs81002844
Exacrs81002844
Varsomers81002844
Maprs81002844
PheGenIrs81002844
hapmaprs81002844
1000 genomesrs81002844
hgdprs81002844
ensemblrs81002844
gopubmedrs81002844
geneviewrs81002844
scholarrs81002844
googlers81002844
pharmgkbrs81002844
gwascentralrs81002844
openSNPrs81002844
23andMers81002844
23andMe allrs81002844
SNP Nexus

SNPshotrs81002844
SNPdbers81002844
MSV3drs81002844
GWAS Ctlgrs81002844
Max Magnitude0
ClinVar
Risk rs81002844(G,T;G,T)
Alt rs81002844(G,T;G,T)
Reference rs81002844(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953884C>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045671.2, RCV000114023.1,