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rs431825371

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs431825371(A;A)
Make rs431825371(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379399
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825371
ebirs431825371
HLIrs431825371
Exacrs431825371
Varsomers431825371
Maprs431825371
PheGenIrs431825371
hapmaprs431825371
1000 genomesrs431825371
hgdprs431825371
ensemblrs431825371
gopubmedrs431825371
geneviewrs431825371
scholarrs431825371
googlers431825371
pharmgkbrs431825371
gwascentralrs431825371
openSNPrs431825371
23andMers431825371
23andMe allrs431825371
SNP Nexus

SNPshotrs431825371
SNPdbers431825371
MSV3drs431825371
GWAS Ctlgrs431825371
Max Magnitude0
ClinVar
Risk rs431825371(A;A)
Alt rs431825371(A;A)
Reference rs431825371(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953536T>A
CLNSRC ClinVar
CLNACC RCV000082995.2, RCV000164349.1,