MCCC1, methylcrotonoyl-CoA carboxylase 1, 56922

N. diseases: 42; N. variants: 57
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10513789
rs10513789
Entrez Id: 56922
Gene Symbol: MCCC1
MCCC1
CUI: C0030567
Disease:
Parkinson Disease 		T 0.800 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs10513789
rs10513789
Entrez Id: 56922
Gene Symbol: MCCC1
MCCC1
CUI: C0030567
Disease:
Parkinson Disease 		T 0.800 GeneticVariation GWASCAT Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011