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rs398122531

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 6 BRCA2 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar


Make rs398122531(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339707
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122531
ebirs398122531
HLIrs398122531
Exacrs398122531
Varsomers398122531
Maprs398122531
PheGenIrs398122531
hapmaprs398122531
1000 genomesrs398122531
hgdprs398122531
ensemblrs398122531
gopubmedrs398122531
geneviewrs398122531
scholarrs398122531
googlers398122531
pharmgkbrs398122531
gwascentralrs398122531
openSNPrs398122531
23andMers398122531
23andMe allrs398122531
SNP Nexus

SNPshotrs398122531
SNPdbers398122531
MSV3drs398122531
GWAS Ctlgrs398122531
Max Magnitude6
ClinVar
Risk rs398122531(;)
Alt rs398122531(;)
Reference rs398122531(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.32913844delC
CLNSRC ClinVar
CLNACC RCV000076930.2,