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rs431825332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs431825332(A;T)
Make rs431825332(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339933
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825332
ebirs431825332
HLIrs431825332
Exacrs431825332
Varsomers431825332
Maprs431825332
PheGenIrs431825332
hapmaprs431825332
1000 genomesrs431825332
hgdprs431825332
ensemblrs431825332
gopubmedrs431825332
geneviewrs431825332
scholarrs431825332
googlers431825332
pharmgkbrs431825332
gwascentralrs431825332
openSNPrs431825332
23andMers431825332
23andMe allrs431825332
SNP Nexus

SNPshotrs431825332
SNPdbers431825332
MSV3drs431825332
GWAS Ctlgrs431825332
Max Magnitude0
ClinVar
Risk rs431825332(T;T)
Alt rs431825332(T;T)
Reference rs431825332(A;A)
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.32914070A>T
CLNSRC ClinVar
CLNACC RCV000082944.2, RCV000164633.1,