MALAT1 and coronary artery disorder: When the term MALAT1 was searched via the ClinVar database [75] (freely available, public archive of human genetic variants and interpretations of their significance to disease) (https://www.ncbi.nlm.nih.gov/clinvar/?term=malat1%5Bgene%5D&redir=gene; accessed on 11 January 2023), 14 records (e.g., ependymoma and glycogen storage disease, type V, Bardet-Biedl syndrome) were found, further suggesting that the lncRNA polymorphisms are associated with various diseases, not only CAD.