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rs431825330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs431825330(-;-)
Make rs431825330(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339733
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825330
ebirs431825330
HLIrs431825330
Exacrs431825330
Varsomers431825330
Maprs431825330
PheGenIrs431825330
hapmaprs431825330
1000 genomesrs431825330
hgdprs431825330
ensemblrs431825330
gopubmedrs431825330
geneviewrs431825330
scholarrs431825330
googlers431825330
pharmgkbrs431825330
gwascentralrs431825330
openSNPrs431825330
23andMers431825330
23andMe allrs431825330
SNP Nexus

SNPshotrs431825330
SNPdbers431825330
MSV3drs431825330
GWAS Ctlgrs431825330
Max Magnitude0
ClinVar
Risk rs431825330(;)
Alt rs431825330(;)
Reference rs431825330(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913870delA
CLNSRC ClinVar
CLNACC RCV000082941.2,