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rs81002847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002847(A;G)
Make rs81002847(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357937
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002847
ebirs81002847
HLIrs81002847
Exacrs81002847
Varsomers81002847
Maprs81002847
PheGenIrs81002847
hapmaprs81002847
1000 genomesrs81002847
hgdprs81002847
ensemblrs81002847
gopubmedrs81002847
geneviewrs81002847
scholarrs81002847
googlers81002847
pharmgkbrs81002847
gwascentralrs81002847
openSNPrs81002847
23andMers81002847
23andMe allrs81002847
SNP Nexus

SNPshotrs81002847
SNPdbers81002847
MSV3drs81002847
GWAS Ctlgrs81002847
Max Magnitude0
ClinVar
Risk rs81002847(G;G)
Alt rs81002847(G;G)
Reference rs81002847(A;A)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32932074A>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045317.3, RCV000077413.4,