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rs398122793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122793(-;-)
Make rs398122793(-;T)
Make rs398122793(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326278
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122793
ebirs398122793
HLIrs398122793
Exacrs398122793
Varsomers398122793
Maprs398122793
PheGenIrs398122793
hapmaprs398122793
1000 genomesrs398122793
hgdprs398122793
ensemblrs398122793
gopubmedrs398122793
geneviewrs398122793
scholarrs398122793
googlers398122793
pharmgkbrs398122793
gwascentralrs398122793
openSNPrs398122793
23andMers398122793
23andMe allrs398122793
SNP Nexus

SNPshotrs398122793
SNPdbers398122793
MSV3drs398122793
GWAS Ctlgrs398122793
Max Magnitude0
ClinVar
Risk rs398122793(T;T)
Alt rs398122793(T;T)
Reference rs398122793(;)
Significance Pathogenic
Disease Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32900415dupT
CLNSRC ClinVar
CLNACC RCV000077742.2, RCV000214392.1,