Have questions? Visit https://www.reddit.com/r/SNPedia

rs431825342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs431825342(-;-)
Make rs431825342(-;T)
Make rs431825342(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340752
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825342
ebirs431825342
HLIrs431825342
Exacrs431825342
Varsomers431825342
Maprs431825342
PheGenIrs431825342
hapmaprs431825342
1000 genomesrs431825342
hgdprs431825342
ensemblrs431825342
gopubmedrs431825342
geneviewrs431825342
scholarrs431825342
googlers431825342
pharmgkbrs431825342
gwascentralrs431825342
openSNPrs431825342
23andMers431825342
23andMe allrs431825342
SNP Nexus

SNPshotrs431825342
SNPdbers431825342
MSV3drs431825342
GWAS Ctlgrs431825342
Max Magnitude0
ClinVar
Risk rs431825342(T;T)
Alt rs431825342(T;T)
Reference rs431825342(;)
Significance Pathogenic
Disease Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32914889dupT
CLNSRC ClinVar
CLNACC RCV000082959.2, RCV000219740.1,