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rs202247818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202247818(A;A)
Make rs202247818(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136256586
GenePCCB
is asnp
is mentioned by
dbSNPrs202247818
ebirs202247818
HLIrs202247818
Exacrs202247818
Varsomers202247818
Maprs202247818
PheGenIrs202247818
hapmaprs202247818
1000 genomesrs202247818
hgdprs202247818
ensemblrs202247818
gopubmedrs202247818
geneviewrs202247818
scholarrs202247818
googlers202247818
pharmgkbrs202247818
gwascentralrs202247818
openSNPrs202247818
23andMers202247818
23andMe allrs202247818
SNP Nexus

SNPshotrs202247818
SNPdbers202247818
MSV3drs202247818
GWAS Ctlgrs202247818
Max Magnitude0
ClinVar
Risk rs202247818(A;A)
Alt rs202247818(A;A)
Reference rs202247818(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135975428G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032132.1,