Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs118204016
rs118204016
ACADVL ; MIR324
0.010 GeneticVariation BEFREE The ACADVL R450H mutation is an uncommon cause of the DCM phenotype that appears to be autosomal recessive. 30840296

2019