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rs202247817

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202247817(G;T)
Make rs202247817(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position136255952
GenePCCB
is asnp
is mentioned by
dbSNPrs202247817
ebirs202247817
HLIrs202247817
Exacrs202247817
Varsomers202247817
Maprs202247817
PheGenIrs202247817
hapmaprs202247817
1000 genomesrs202247817
hgdprs202247817
ensemblrs202247817
gopubmedrs202247817
geneviewrs202247817
scholarrs202247817
googlers202247817
pharmgkbrs202247817
gwascentralrs202247817
openSNPrs202247817
23andMers202247817
23andMe allrs202247817
SNP Nexus

SNPshotrs202247817
SNPdbers202247817
MSV3drs202247817
GWAS Ctlgrs202247817
Max Magnitude0
ClinVar
Risk rs202247817(T;T)
Alt rs202247817(T;T)
Reference rs202247817(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135974794G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032131.1,