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rs81002809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002809(A;A)
Make rs81002809(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357930
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002809
ebirs81002809
HLIrs81002809
Exacrs81002809
Varsomers81002809
Maprs81002809
PheGenIrs81002809
hapmaprs81002809
1000 genomesrs81002809
hgdprs81002809
ensemblrs81002809
gopubmedrs81002809
geneviewrs81002809
scholarrs81002809
googlers81002809
pharmgkbrs81002809
gwascentralrs81002809
openSNPrs81002809
23andMers81002809
23andMe allrs81002809
SNP Nexus

SNPshotrs81002809
SNPdbers81002809
MSV3drs81002809
GWAS Ctlgrs81002809
Max Magnitude0
ClinVar
Risk rs81002809(A;A)
Alt rs81002809(A;A)
Reference rs81002809(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32932067G>A
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045313.2, RCV000077411.3, RCV000239169.1,