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rs81002873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002873(A;A)
Make rs81002873(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362694
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002873
ebirs81002873
HLIrs81002873
Exacrs81002873
Varsomers81002873
Maprs81002873
PheGenIrs81002873
hapmaprs81002873
1000 genomesrs81002873
hgdprs81002873
ensemblrs81002873
gopubmedrs81002873
geneviewrs81002873
scholarrs81002873
googlers81002873
pharmgkbrs81002873
gwascentralrs81002873
openSNPrs81002873
23andMers81002873
23andMe allrs81002873
SNP Nexus

SNPshotrs81002873
SNPdbers81002873
MSV3drs81002873
GWAS Ctlgrs81002873
Max Magnitude0
ClinVar
Risk rs81002873(A;A)
Alt rs81002873(A;A)
Reference rs81002873(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32936831G>A
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045363.2, RCV000077419.3, RCV000131083.2, RCV000235799.1,