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rs81002802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs81002802(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379914
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002802
ebirs81002802
HLIrs81002802
Exacrs81002802
Varsomers81002802
Maprs81002802
PheGenIrs81002802
hapmaprs81002802
1000 genomesrs81002802
hgdprs81002802
ensemblrs81002802
gopubmedrs81002802
geneviewrs81002802
scholarrs81002802
googlers81002802
pharmgkbrs81002802
gwascentralrs81002802
openSNPrs81002802
23andMers81002802
23andMe allrs81002802
SNP Nexus

SNPshotrs81002802
SNPdbers81002802
MSV3drs81002802
GWAS Ctlgrs81002802
Max Magnitude6
ClinVar
Risk rs81002802(A,T;A,T)
Alt rs81002802(A,T;A,T)
Reference rs81002802(G;G)
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.32954051G>A; NC_000013.10:g.32954051G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045721.2, RCV000114050.2, RCV000045722.2, RCV000114051.1,