Have questions? Visit https://www.reddit.com/r/SNPedia

rs81002796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002796(G;T)
Make rs81002796(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32316528
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002796
ebirs81002796
HLIrs81002796
Exacrs81002796
Varsomers81002796
Maprs81002796
PheGenIrs81002796
hapmaprs81002796
1000 genomesrs81002796
hgdprs81002796
ensemblrs81002796
gopubmedrs81002796
geneviewrs81002796
scholarrs81002796
googlers81002796
pharmgkbrs81002796
gwascentralrs81002796
openSNPrs81002796
23andMers81002796
23andMe allrs81002796
SNP Nexus

SNPshotrs81002796
SNPdbers81002796
MSV3drs81002796
GWAS Ctlgrs81002796
Max Magnitude0
ClinVar
Risk rs81002796(A,T;A,T)
Alt rs81002796(A,T;A,T)
Reference rs81002796(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32890665G>A; NC_000013.10:g.32890665G>C; NC_000013.10:g.32890665G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045021.2, RCV000077381.3, RCV000218090.1, RCV000217482.1, RCV000239221.1, RCV000045022.3, RCV000077382.3, RCV000162894.1,