Disease: Medium-chain acyl-coenzyme A dehydrogenase deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773507991
rs773507991
Entrez Id: 23263
Gene Symbol: MCF2L
MCF2L
CUI: C0220710
Disease:
Medium-chain acyl-coenzyme A dehydrogenase deficiency 		0.010 GeneticVariation BEFREE To date, more than 67 mutations have been reported to cause MCADD with a single allele, c.985A>G, being the most common in patients of northwestern European descent. 20567907 2010