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rs81002837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002837(G;T)
Make rs81002837(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363534
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002837
ebirs81002837
HLIrs81002837
Exacrs81002837
Varsomers81002837
Maprs81002837
PheGenIrs81002837
hapmaprs81002837
1000 genomesrs81002837
hgdprs81002837
ensemblrs81002837
gopubmedrs81002837
geneviewrs81002837
scholarrs81002837
googlers81002837
pharmgkbrs81002837
gwascentralrs81002837
openSNPrs81002837
23andMers81002837
23andMe allrs81002837
SNP Nexus

SNPshotrs81002837
SNPdbers81002837
MSV3drs81002837
GWAS Ctlgrs81002837
Max Magnitude0
ClinVar
Risk rs81002837(A,T;A,T)
Alt rs81002837(A,T;A,T)
Reference rs81002837(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32937671G>A; NC_000013.10:g.32937671G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031737.3, RCV000045477.4, RCV000166511.1, RCV000212272.1, RCV000045478.2, RCV000113904.1,