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rs431825321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs431825321(-;-)
Make rs431825321(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338874
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825321
ebirs431825321
HLIrs431825321
Exacrs431825321
Varsomers431825321
Maprs431825321
PheGenIrs431825321
hapmaprs431825321
1000 genomesrs431825321
hgdprs431825321
ensemblrs431825321
gopubmedrs431825321
geneviewrs431825321
scholarrs431825321
googlers431825321
pharmgkbrs431825321
gwascentralrs431825321
openSNPrs431825321
23andMers431825321
23andMe allrs431825321
SNP Nexus

SNPshotrs431825321
SNPdbers431825321
MSV3drs431825321
GWAS Ctlgrs431825321
Max Magnitude0
ClinVar
Risk rs431825321(;)
Alt rs431825321(;)
Reference rs431825321(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.32913011delC
CLNSRC ClinVar
CLNACC RCV000082929.2,