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rs431825325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs431825325(-;-)
Make rs431825325(-;G)
Make rs431825325(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339331
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825325
ebirs431825325
HLIrs431825325
Exacrs431825325
Varsomers431825325
Maprs431825325
PheGenIrs431825325
hapmaprs431825325
1000 genomesrs431825325
hgdprs431825325
ensemblrs431825325
gopubmedrs431825325
geneviewrs431825325
scholarrs431825325
googlers431825325
pharmgkbrs431825325
gwascentralrs431825325
openSNPrs431825325
23andMers431825325
23andMe allrs431825325
SNP Nexus

SNPshotrs431825325
SNPdbers431825325
MSV3drs431825325
GWAS Ctlgrs431825325
Max Magnitude0
ClinVar
Risk rs431825325(G;G)
Alt rs431825325(G;G)
Reference rs431825325(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32913468_32913469insG
CLNSRC ClinVar
CLNACC RCV000082934.2, RCV000122912.1,