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

rs81002806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002806(A;G)
Make rs81002806(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370560
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002806
ebirs81002806
HLIrs81002806
Exacrs81002806
Varsomers81002806
Maprs81002806
PheGenIrs81002806
hapmaprs81002806
1000 genomesrs81002806
hgdprs81002806
ensemblrs81002806
gopubmedrs81002806
geneviewrs81002806
scholarrs81002806
googlers81002806
pharmgkbrs81002806
gwascentralrs81002806
openSNPrs81002806
23andMers81002806
23andMe allrs81002806
SNP Nexus

SNPshotrs81002806
SNPdbers81002806
MSV3drs81002806
GWAS Ctlgrs81002806
Max Magnitude0
ClinVar
Risk rs81002806(G;G)
Alt rs81002806(G;G)
Reference rs81002806(A;A)
Significance Untested
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.32944697A>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045535.2, RCV000113945.1,