MCCC2, methylcrotonoyl-CoA carboxylase 2, 64087

N. diseases: 50; N. variants: 50
Disease: 3-methylcrotonyl CoA carboxylase 2 deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119103219
rs119103219
Entrez Id: 64087
Gene Symbol: MCCC2
MCCC2
CUI: C1859499
Disease:
3-methylcrotonyl CoA carboxylase 2 deficiency 		0.800 GeneticVariation UNIPROT
dbSNP: rs119103219
rs119103219
Entrez Id: 64087
Gene Symbol: MCCC2
MCCC2
CUI: C1859499
Disease:
3-methylcrotonyl CoA carboxylase 2 deficiency 		C 0.800 CausalMutation CLINVAR