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rs398122762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122762(-;-)
Make rs398122762(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337681
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122762
ebirs398122762
HLIrs398122762
Exacrs398122762
Varsomers398122762
Maprs398122762
PheGenIrs398122762
hapmaprs398122762
1000 genomesrs398122762
hgdprs398122762
ensemblrs398122762
gopubmedrs398122762
geneviewrs398122762
scholarrs398122762
googlers398122762
pharmgkbrs398122762
gwascentralrs398122762
openSNPrs398122762
23andMers398122762
23andMe allrs398122762
SNP Nexus

SNPshotrs398122762
SNPdbers398122762
MSV3drs398122762
GWAS Ctlgrs398122762
Max Magnitude0
ClinVar
Risk rs398122762(;)
Alt rs398122762(;)
Reference rs398122762(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911818delC
CLNSRC ClinVar
CLNACC RCV000077705.2,