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rs81002863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002863(A;G)
Make rs81002863(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346825
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002863
ebirs81002863
HLIrs81002863
Exacrs81002863
Varsomers81002863
Maprs81002863
PheGenIrs81002863
hapmaprs81002863
1000 genomesrs81002863
hgdprs81002863
ensemblrs81002863
gopubmedrs81002863
geneviewrs81002863
scholarrs81002863
googlers81002863
pharmgkbrs81002863
gwascentralrs81002863
openSNPrs81002863
23andMers81002863
23andMe allrs81002863
SNP Nexus

SNPshotrs81002863
SNPdbers81002863
MSV3drs81002863
GWAS Ctlgrs81002863
Max Magnitude0
ClinVar
Risk rs81002863(G;G)
Alt rs81002863(G;G)
Reference rs81002863(A;A)
Significance Other
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.32920962A>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045090.2, RCV000083132.4,