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rs81002895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002895(A;G)
Make rs81002895(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398160
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002895
ebirs81002895
HLIrs81002895
Exacrs81002895
Varsomers81002895
Maprs81002895
PheGenIrs81002895
hapmaprs81002895
1000 genomesrs81002895
hgdprs81002895
ensemblrs81002895
gopubmedrs81002895
geneviewrs81002895
scholarrs81002895
googlers81002895
pharmgkbrs81002895
gwascentralrs81002895
openSNPrs81002895
23andMers81002895
23andMe allrs81002895
SNP Nexus

SNPshotrs81002895
SNPdbers81002895
MSV3drs81002895
GWAS Ctlgrs81002895
Max Magnitude0
ClinVar
Risk rs81002895(G;G)
Alt rs81002895(G;G)
Reference rs81002895(A;A)
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.32972297A>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045879.2, RCV000114145.1,