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rs374722096

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374722096(C;T)
Make rs374722096(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position136293784
GenePCCB
is asnp
is mentioned by
dbSNPrs374722096
ebirs374722096
HLIrs374722096
Exacrs374722096
Varsomers374722096
Maprs374722096
PheGenIrs374722096
hapmaprs374722096
1000 genomesrs374722096
hgdprs374722096
ensemblrs374722096
gopubmedrs374722096
geneviewrs374722096
scholarrs374722096
googlers374722096
pharmgkbrs374722096
gwascentralrs374722096
openSNPrs374722096
23andMers374722096
23andMe allrs374722096
SNP Nexus

SNPshotrs374722096
SNPdbers374722096
MSV3drs374722096
GWAS Ctlgrs374722096
Max Magnitude0
ClinVar
Risk rs374722096(T;T)
Alt rs374722096(T;T)
Reference rs374722096(C;C)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136012626C>T
CLNSRC
CLNACC RCV000179767.1,