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rs431825381

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs431825381(-;-)
Make rs431825381(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32398458
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825381
ebirs431825381
HLIrs431825381
Exacrs431825381
Varsomers431825381
Maprs431825381
PheGenIrs431825381
hapmaprs431825381
1000 genomesrs431825381
hgdprs431825381
ensemblrs431825381
gopubmedrs431825381
geneviewrs431825381
scholarrs431825381
googlers431825381
pharmgkbrs431825381
gwascentralrs431825381
openSNPrs431825381
23andMers431825381
23andMe allrs431825381
SNP Nexus

SNPshotrs431825381
SNPdbers431825381
MSV3drs431825381
GWAS Ctlgrs431825381
Max Magnitude0
ClinVar
Risk rs431825381(;)
Alt rs431825381(;)
Reference rs431825381(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer not specified Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not specified Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32972595delA
CLNSRC
CLNACC RCV000083011.2, RCV000160314.2, RCV000165269.2, RCV000204290.1,