rs77931234, ACADM

N. diseases: 3
Disease: Sudden infant death syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sudden infant death syndrome
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