Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434278
rs121434278
Entrez Id: 34
Gene Symbol: ACADM
ACADM
CUI: C0038644
Disease:
Sudden infant death syndrome
0.010 GeneticVariation BEFREE We investigated the incidence of a rare MCAD mutation (G583A) in a large population of SIDS patients. 9160189 1997
dbSNP: rs77931234
rs77931234
Entrez Id: 34
Gene Symbol: ACADM
ACADM
CUI: C0038644
Disease:
Sudden infant death syndrome
0.010 GeneticVariation BEFREE The A985 to G mutation of the medium-chain acyl-CoA dehydrogenase gene and sudden infant death syndrome in Normandy. 8640038 1996