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rs202247822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs202247822(C;C)
Make rs202247822(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position136329962
GenePCCB
is asnp
is mentioned by
dbSNPrs202247822
ebirs202247822
HLIrs202247822
Exacrs202247822
Varsomers202247822
Maprs202247822
PheGenIrs202247822
hapmaprs202247822
1000 genomesrs202247822
hgdprs202247822
ensemblrs202247822
gopubmedrs202247822
geneviewrs202247822
scholarrs202247822
googlers202247822
pharmgkbrs202247822
gwascentralrs202247822
openSNPrs202247822
23andMers202247822
23andMe allrs202247822
SNP Nexus

SNPshotrs202247822
SNPdbers202247822
MSV3drs202247822
GWAS Ctlgrs202247822
Max Magnitude0
ClinVar
Risk rs202247822(C;C)
Alt rs202247822(C;C)
Reference rs202247822(T;T)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136048804T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000032129.1,