Disease: Acute myocardial infarction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs754889760
rs754889760
Entrez Id: 1375;386593
Gene Symbol: CPT1B;CHKB-CPT1B
CPT1B;CHKB-CPT1B
CUI: C0155626
Disease:
Acute myocardial infarction 		0.010 GeneticVariation BEFREE The homozygous genotype (AA) of CPT2 variant V368I had significantly less blood carnitine in AMI patients. 23566841 2013