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rs81002885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs81002885(C;C)
Make rs81002885(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32316529
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002885
ebirs81002885
HLIrs81002885
Exacrs81002885
Varsomers81002885
Maprs81002885
PheGenIrs81002885
hapmaprs81002885
1000 genomesrs81002885
hgdprs81002885
ensemblrs81002885
gopubmedrs81002885
geneviewrs81002885
scholarrs81002885
googlers81002885
pharmgkbrs81002885
gwascentralrs81002885
openSNPrs81002885
23andMers81002885
23andMe allrs81002885
SNP Nexus

SNPshotrs81002885
SNPdbers81002885
MSV3drs81002885
GWAS Ctlgrs81002885
Max Magnitude0
ClinVar
Risk rs81002885(A,C;A,C)
Alt rs81002885(A,C;A,C)
Reference rs81002885(T;T)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32890666T>A; NC_000013.10:g.32890666T>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045023.2, RCV000113080.1, RCV000045024.3, RCV000113081.1,