Publication | Open Access

Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk

EpidemiologyCardiovascular DiseaseMyocardial Infarction RiskGenetic EpidemiologyCandidate Causal VariantTotal CholesterolCardiologyBiostatisticsPublic HealthMedicineAtherosclerosisCardiovascular GeneticsCoronary Artery DiseaseAcute Myocardial InfarctionMyocardial Infarction