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rs81002813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002813(G;T)
Make rs81002813(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376796
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002813
ebirs81002813
HLIrs81002813
Exacrs81002813
Varsomers81002813
Maprs81002813
PheGenIrs81002813
hapmaprs81002813
1000 genomesrs81002813
hgdprs81002813
ensemblrs81002813
gopubmedrs81002813
geneviewrs81002813
scholarrs81002813
googlers81002813
pharmgkbrs81002813
gwascentralrs81002813
openSNPrs81002813
23andMers81002813
23andMe allrs81002813
SNP Nexus

SNPshotrs81002813
SNPdbers81002813
MSV3drs81002813
GWAS Ctlgrs81002813
Max Magnitude0
ClinVar
Risk rs81002813(A,T;A,T)
Alt rs81002813(A,T;A,T)
Reference rs81002813(G;G)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32950933G>A; NC_000013.10:g.32950933G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031765.6, RCV000045616.2, RCV000045617.2, RCV000113993.1,