Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057516979
rs1057516979
Entrez Id: 37;1742
Gene Symbol: ACADVL;DLG4
ACADVL;DLG4
CUI: C3887523
Disease:
Very long chain acyl-CoA dehydrogenase deficiency
T 0.700 GeneticVariation CLINVAR Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States. 26385305 2015