SENCR and coronary artery disorder: Single nucleotide polymorphisms are the sequence variants with sometimes, deleterious effects on the expression and function of the genes and so, may involve in the pathogenesis of human diseases.22,23 The examples of such functional SNPs was reported for exon 2 and 3 of the SENCR gene.9 To the best of our knowledge, this the first study examined the association of the rs555172 SNP of the SENCR lncRNA with the susceptibility to CAD.