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rs431825288

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs431825288(C;G)
Make rs431825288(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333385
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825288
ebirs431825288
HLIrs431825288
Exacrs431825288
Varsomers431825288
Maprs431825288
PheGenIrs431825288
hapmaprs431825288
1000 genomesrs431825288
hgdprs431825288
ensemblrs431825288
gopubmedrs431825288
geneviewrs431825288
scholarrs431825288
googlers431825288
pharmgkbrs431825288
gwascentralrs431825288
openSNPrs431825288
23andMers431825288
23andMe allrs431825288
SNP Nexus

SNPshotrs431825288
SNPdbers431825288
MSV3drs431825288
GWAS Ctlgrs431825288
Max Magnitude0
ClinVar
Risk rs431825288(G;G)
Alt rs431825288(G;G)
Reference rs431825288(C;C)
Significance Probable-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.32907522C>G; NC_000013.10:g.32907522C>T
CLNSRC ClinVar
CLNACC RCV000082893.2, RCV000220348.1,