Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs765793260
rs765793260
ACADM
G 0.700 CausalMutation CLINVAR MCAD deficiency in Denmark. 22542437

2012
dbSNP: rs765793260
rs765793260
ACADM
G 0.700 CausalMutation CLINVAR Newborn screening for medium chain acyl-CoA dehydrogenase deficiency in England: prevalence, predictive value and test validity based on 1.5 million screened babies. 22166308

2011