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rs431825307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs431825307(A;A)
Make rs431825307(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337832
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825307
ebirs431825307
HLIrs431825307
Exacrs431825307
Varsomers431825307
Maprs431825307
PheGenIrs431825307
hapmaprs431825307
1000 genomesrs431825307
hgdprs431825307
ensemblrs431825307
gopubmedrs431825307
geneviewrs431825307
scholarrs431825307
googlers431825307
pharmgkbrs431825307
gwascentralrs431825307
openSNPrs431825307
23andMers431825307
23andMe allrs431825307
SNP Nexus

SNPshotrs431825307
SNPdbers431825307
MSV3drs431825307
GWAS Ctlgrs431825307
Max Magnitude0
ClinVar
Risk rs431825307(A;A)
Alt rs431825307(A;A)
Reference rs431825307(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.32911969C>A
CLNSRC ClinVar
CLNACC RCV000082912.2,