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rs431825292

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs431825292(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336446
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825292
dbSNP (classic)rs431825292
ClinGenrs431825292
ebirs431825292
HLIrs431825292
Exacrs431825292
Gnomadrs431825292
Varsomers431825292
LitVarrs431825292
Maprs431825292
PheGenIrs431825292
Biobankrs431825292
1000 genomesrs431825292
hgdprs431825292
ensemblrs431825292
geneviewrs431825292
scholarrs431825292
googlers431825292
pharmgkbrs431825292
gwascentralrs431825292
openSNPrs431825292
23andMers431825292
SNPshotrs431825292
SNPdbers431825292
MSV3drs431825292
GWAS Ctlgrs431825292
Max Magnitude6
ClinVar
Risk rs431825292(A;A)
Alt rs431825292(A;A)
Reference Rs431825292(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910583dupA
CLNSRC ClinVar
CLNACC RCV000082897.4,