Variant: rs12541758

present in Gene: LOC392232 present in Chromosome: 8 Position on Chromosome: 72230147 Alleles of this Variant: C/T

rs12541758 in LOC392232 gene and Coronary Artery Disease PMID 26708285 2016 Several SNPs, including the rs7421388 (PLCL1) and rs12541758 (TRPA1) displaying a suggestive GWAS association (P < 1 × 10(-5)) with CAD as well as rs41411047 (RNF13), rs32793 (PDZD2) and rs4739066 (YTHDF3), similarly showing weak association with MI, were confirmed in an independent dataset.