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rs81002805

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs81002805(C;C)
Make rs81002805(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319327
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002805
ebirs81002805
HLIrs81002805
Exacrs81002805
Varsomers81002805
Maprs81002805
PheGenIrs81002805
hapmaprs81002805
1000 genomesrs81002805
hgdprs81002805
ensemblrs81002805
gopubmedrs81002805
geneviewrs81002805
scholarrs81002805
googlers81002805
pharmgkbrs81002805
gwascentralrs81002805
openSNPrs81002805
23andMers81002805
23andMe allrs81002805
SNP Nexus

SNPshotrs81002805
SNPdbers81002805
MSV3drs81002805
GWAS Ctlgrs81002805
Max Magnitude0
ClinVar
Risk rs81002805(C;C)
Alt rs81002805(C;C)
Reference rs81002805(T;T)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32893464T>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044128.2, RCV000113397.1, RCV000131849.2,