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rs81002843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs81002843(G;G)
Make rs81002843(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356611
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002843
ebirs81002843
HLIrs81002843
Exacrs81002843
Varsomers81002843
Maprs81002843
PheGenIrs81002843
hapmaprs81002843
1000 genomesrs81002843
hgdprs81002843
ensemblrs81002843
gopubmedrs81002843
geneviewrs81002843
scholarrs81002843
googlers81002843
pharmgkbrs81002843
gwascentralrs81002843
openSNPrs81002843
23andMers81002843
23andMe allrs81002843
SNP Nexus

SNPshotrs81002843
SNPdbers81002843
MSV3drs81002843
GWAS Ctlgrs81002843
Max Magnitude0
ClinVar
Risk rs81002843(G;G)
Alt rs81002843(G;G)
Reference rs81002843(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32930748T>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045261.3, RCV000113793.1,