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rs81002883

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002883(A;A)
Make rs81002883(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380146
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002883
ebirs81002883
HLIrs81002883
Exacrs81002883
Varsomers81002883
Maprs81002883
PheGenIrs81002883
hapmaprs81002883
1000 genomesrs81002883
hgdprs81002883
ensemblrs81002883
gopubmedrs81002883
geneviewrs81002883
scholarrs81002883
googlers81002883
pharmgkbrs81002883
gwascentralrs81002883
openSNPrs81002883
23andMers81002883
23andMe allrs81002883
SNP Nexus

SNPshotrs81002883
SNPdbers81002883
MSV3drs81002883
GWAS Ctlgrs81002883
Max Magnitude0
ClinVar
Risk rs81002883(A,C;A,C)
Alt rs81002883(A,C;A,C)
Reference rs81002883(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.32954283G>A; NC_000013.10:g.32954283G>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045761.2, RCV000114075.1, RCV000083002.2,