ZC3HC1 and coronary artery disorder: With respect to this, the genetic variant rs11556924 (C > T) that is located at 7q32.2 and encodes a non-synonymous change (R363H) in the ZC3HC1 (zinc finger, C3HC-type containing 1) gene, seems to be one of the most significant signals associated with CAD in non-rheumatic Caucasian individuals [9].