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rs81002853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002853(A;G)
Make rs81002853(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326240
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002853
ebirs81002853
HLIrs81002853
Exacrs81002853
Varsomers81002853
Maprs81002853
PheGenIrs81002853
hapmaprs81002853
1000 genomesrs81002853
hgdprs81002853
ensemblrs81002853
gopubmedrs81002853
geneviewrs81002853
scholarrs81002853
googlers81002853
pharmgkbrs81002853
gwascentralrs81002853
openSNPrs81002853
23andMers81002853
23andMe allrs81002853
SNP Nexus

SNPshotrs81002853
SNPdbers81002853
MSV3drs81002853
GWAS Ctlgrs81002853
Max Magnitude0
ClinVar
Risk rs81002853(G;G)
Alt rs81002853(G;G)
Reference rs81002853(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32900377A>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031504.7, RCV000044488.2, RCV000131855.2,