Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553127172
rs1553127172
ACADM
G 0.700 CausalMutation CLINVAR Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. 20434380

2010
dbSNP: rs1553127172
rs1553127172
ACADM
G 0.700 CausalMutation CLINVAR Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene. 8198141

1994