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rs81002882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002882(G;T)
Make rs81002882(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379516
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002882
ebirs81002882
HLIrs81002882
Exacrs81002882
Varsomers81002882
Maprs81002882
PheGenIrs81002882
hapmaprs81002882
1000 genomesrs81002882
hgdprs81002882
ensemblrs81002882
gopubmedrs81002882
geneviewrs81002882
scholarrs81002882
googlers81002882
pharmgkbrs81002882
gwascentralrs81002882
openSNPrs81002882
23andMers81002882
23andMe allrs81002882
SNP Nexus

SNPshotrs81002882
SNPdbers81002882
MSV3drs81002882
GWAS Ctlgrs81002882
Max Magnitude0
ClinVar
Risk rs81002882(A,T;A,T)
Alt rs81002882(A,T;A,T)
Reference rs81002882(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32953653G>A; NC_000013.10:g.32953653G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045667.2, RCV000031781.5, RCV000074557.4, RCV000131051.2, RCV000213611.1,