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rs81002820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002820(C;C)
Make rs81002820(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32329442
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002820
ebirs81002820
HLIrs81002820
Exacrs81002820
Varsomers81002820
Maprs81002820
PheGenIrs81002820
hapmaprs81002820
1000 genomesrs81002820
hgdprs81002820
ensemblrs81002820
gopubmedrs81002820
geneviewrs81002820
scholarrs81002820
googlers81002820
pharmgkbrs81002820
gwascentralrs81002820
openSNPrs81002820
23andMers81002820
23andMe allrs81002820
SNP Nexus

SNPshotrs81002820
SNPdbers81002820
MSV3drs81002820
GWAS Ctlgrs81002820
Max Magnitude0
ClinVar
Risk rs81002820(A,C,T;A,C,T)
Alt rs81002820(A,C,T;A,C,T)
Reference rs81002820(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32903579G>A; NC_000013.10:g.32903579G>C; NC_000013.10:g.32903579G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044905.2, RCV000044906.2, RCV000113919.1, RCV000044907.2,