Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908419
rs121908419
ACAD8
A 0.700 GeneticVariation CLINVAR Targeted metabolomics in the expanded newborn screening for inborn errors of metabolism. 25689098

2015
dbSNP: rs121908419
rs121908419
ACAD8
A 0.700 GeneticVariation CLINVAR Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency. 17304052

2007
dbSNP: rs121908419
rs121908419
ACAD8
A 0.700 CausalMutation CLINVAR