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rs398123462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123462(A;A)
Make rs398123462(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position136250377
GenePCCB
is asnp
is mentioned by
dbSNPrs398123462
ebirs398123462
HLIrs398123462
Exacrs398123462
Varsomers398123462
Maprs398123462
PheGenIrs398123462
hapmaprs398123462
1000 genomesrs398123462
hgdprs398123462
ensemblrs398123462
gopubmedrs398123462
geneviewrs398123462
scholarrs398123462
googlers398123462
pharmgkbrs398123462
gwascentralrs398123462
openSNPrs398123462
23andMers398123462
23andMe allrs398123462
SNP Nexus

SNPshotrs398123462
SNPdbers398123462
MSV3drs398123462
GWAS Ctlgrs398123462
Max Magnitude0
ClinVar
Risk rs398123462(A;A)
Alt rs398123462(A;A)
Reference rs398123462(T;T)
Significance Pathogenic
Disease not provided Propionic acidemia
Variation info
Gene PCCB
CLNDBN not provided Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135969219T>A
CLNSRC ClinVar Emory University
CLNACC RCV000079093.3, RCV000173152.1,