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rs398123460

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123460(A;A)
Make rs398123460(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136250559
GenePCCB
is asnp
is mentioned by
dbSNPrs398123460
ebirs398123460
HLIrs398123460
Exacrs398123460
Varsomers398123460
Maprs398123460
PheGenIrs398123460
hapmaprs398123460
1000 genomesrs398123460
hgdprs398123460
ensemblrs398123460
gopubmedrs398123460
geneviewrs398123460
scholarrs398123460
googlers398123460
pharmgkbrs398123460
gwascentralrs398123460
openSNPrs398123460
23andMers398123460
23andMe allrs398123460
SNP Nexus

SNPshotrs398123460
SNPdbers398123460
MSV3drs398123460
GWAS Ctlgrs398123460
Max Magnitude0
ClinVar
Risk rs398123460(A;A)
Alt rs398123460(A;A)
Reference rs398123460(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.135969401G>A
CLNSRC ClinVar
CLNACC RCV000079091.3, RCV000173154.1,