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rs202247820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202247820(C;T)
Make rs202247820(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position136328854
GenePCCB
is asnp
is mentioned by
dbSNPrs202247820
ebirs202247820
HLIrs202247820
Exacrs202247820
Varsomers202247820
Maprs202247820
PheGenIrs202247820
hapmaprs202247820
1000 genomesrs202247820
hgdprs202247820
ensemblrs202247820
gopubmedrs202247820
geneviewrs202247820
scholarrs202247820
googlers202247820
pharmgkbrs202247820
gwascentralrs202247820
openSNPrs202247820
23andMers202247820
23andMe allrs202247820
SNP Nexus

SNPshotrs202247820
SNPdbers202247820
MSV3drs202247820
GWAS Ctlgrs202247820
Max Magnitude0
ClinVar
Risk rs202247820(T;T)
Alt rs202247820(T;T)
Reference rs202247820(C;C)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136047696C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032127.1,