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rs81002840

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002840(A;A)
Make rs81002840(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319330
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002840
ebirs81002840
HLIrs81002840
Exacrs81002840
Varsomers81002840
Maprs81002840
PheGenIrs81002840
hapmaprs81002840
1000 genomesrs81002840
hgdprs81002840
ensemblrs81002840
gopubmedrs81002840
geneviewrs81002840
scholarrs81002840
googlers81002840
pharmgkbrs81002840
gwascentralrs81002840
openSNPrs81002840
23andMers81002840
23andMe allrs81002840
SNP Nexus

SNPshotrs81002840
SNPdbers81002840
MSV3drs81002840
GWAS Ctlgrs81002840
Max Magnitude0
ClinVar
Risk rs81002840(A,C;A,C)
Alt rs81002840(A,C;A,C)
Reference rs81002840(G;G)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893467G>A; NC_000013.10:g.32893467G>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044130.3, RCV000077294.4, RCV000216220.1, RCV000044131.2,