Tseng et al. analysed 258 candidate SNPs with a potential functional role in CAD (TGFβR1: 24 SNPs; TGFβR2: 125 SNPs; TGFβR3: 109 SNPs), but only a single SNP in TGFβR2 (rs9838682) remained statistically significant [61]. The gene discussed is TGFBR2; the disease is coronary artery disorder.