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rs81002860

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002860(G;T)
Make rs81002860(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362522
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002860
ebirs81002860
HLIrs81002860
Exacrs81002860
Varsomers81002860
Maprs81002860
PheGenIrs81002860
hapmaprs81002860
1000 genomesrs81002860
hgdprs81002860
ensemblrs81002860
gopubmedrs81002860
geneviewrs81002860
scholarrs81002860
googlers81002860
pharmgkbrs81002860
gwascentralrs81002860
openSNPrs81002860
23andMers81002860
23andMe allrs81002860
SNP Nexus

SNPshotrs81002860
SNPdbers81002860
MSV3drs81002860
GWAS Ctlgrs81002860
Max Magnitude0
ClinVar
Risk rs81002860(T;T)
Alt rs81002860(T;T)
Reference rs81002860(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.32936659G>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045320.2, RCV000113825.1,