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rs431825323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs431825323(-;-)
Make rs431825323(-;GA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339291
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825323
ebirs431825323
HLIrs431825323
Exacrs431825323
Varsomers431825323
Maprs431825323
PheGenIrs431825323
hapmaprs431825323
1000 genomesrs431825323
hgdprs431825323
ensemblrs431825323
gopubmedrs431825323
geneviewrs431825323
scholarrs431825323
googlers431825323
pharmgkbrs431825323
gwascentralrs431825323
openSNPrs431825323
23andMers431825323
23andMe allrs431825323
SNP Nexus

SNPshotrs431825323
SNPdbers431825323
MSV3drs431825323
GWAS Ctlgrs431825323
Max Magnitude0
ClinVar
Risk rs431825323(;)
Alt rs431825323(;)
Reference rs431825323(AG;AG)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913428_32913429delGA
CLNSRC ClinVar
CLNACC RCV000082932.2, RCV000165590.1,