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rs431825313

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AAAA) 6 BRCA2 variant considered pathogenic for breast cancer
(AAAA;AAAA) 0 common in clinvar


Make rs431825313(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338211
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825313
dbSNP (classic)rs431825313
ClinGenrs431825313
ebirs431825313
HLIrs431825313
Exacrs431825313
Gnomadrs431825313
Varsomers431825313
LitVarrs431825313
Maprs431825313
PheGenIrs431825313
Biobankrs431825313
1000 genomesrs431825313
hgdprs431825313
ensemblrs431825313
geneviewrs431825313
scholarrs431825313
googlers431825313
pharmgkbrs431825313
gwascentralrs431825313
openSNPrs431825313
23andMers431825313
SNPshotrs431825313
SNPdbers431825313
MSV3drs431825313
GWAS Ctlgrs431825313
Merged fromRs886038097
Max Magnitude6

This appears to be a historic SNP, present in older but not newer versions of dbSNP. It appears to have been replaced by rs80359406.

ClinVar
Risk rs431825313(-;-)
Alt rs431825313(-;-)
Reference Rs431825313(AAAA;AAAA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912349_32912352delAAAA
CLNSRC ClinVar
CLNACC RCV000241173.2,