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rs431825338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs431825338(-;-)
Make rs431825338(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340566
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825338
ebirs431825338
HLIrs431825338
Exacrs431825338
Varsomers431825338
Maprs431825338
PheGenIrs431825338
hapmaprs431825338
1000 genomesrs431825338
hgdprs431825338
ensemblrs431825338
gopubmedrs431825338
geneviewrs431825338
scholarrs431825338
googlers431825338
pharmgkbrs431825338
gwascentralrs431825338
openSNPrs431825338
23andMers431825338
23andMe allrs431825338
SNP Nexus

SNPshotrs431825338
SNPdbers431825338
MSV3drs431825338
GWAS Ctlgrs431825338
Max Magnitude0
ClinVar
Risk rs431825338(;)
Alt rs431825338(;)
Reference rs431825338(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not specified
Reversed 0
HGVS NC_000013.10:g.32914703delA
CLNSRC ClinVar
CLNACC RCV000082955.2, RCV000238665.1,