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rs398123464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123464(A;A)
Make rs398123464(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136250378
GenePCCB
is asnp
is mentioned by
dbSNPrs398123464
ebirs398123464
HLIrs398123464
Exacrs398123464
Varsomers398123464
Maprs398123464
PheGenIrs398123464
hapmaprs398123464
1000 genomesrs398123464
hgdprs398123464
ensemblrs398123464
gopubmedrs398123464
geneviewrs398123464
scholarrs398123464
googlers398123464
pharmgkbrs398123464
gwascentralrs398123464
openSNPrs398123464
23andMers398123464
23andMe allrs398123464
SNP Nexus

SNPshotrs398123464
SNPdbers398123464
MSV3drs398123464
GWAS Ctlgrs398123464
Max Magnitude0
ClinVar
Risk rs398123464(A;A)
Alt rs398123464(A;A)
Reference rs398123464(G;G)
Significance Pathogenic
Disease not provided Propionic acidemia
Variation info
Gene PCCB
CLNDBN not provided Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135969220G>A
CLNSRC ClinVar Emory University
CLNACC RCV000079095.3, RCV000173153.1,