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Table 1 SNPs associated with CHD in genome-wide association studies

From: Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record

SNP Chr. Gene Risk allele ORs (95% CI) Risk allele frequency
      Reported Observed
rs10757278 9 CDKN2A/2B G 1.28 (1.22, 1.35) 0.45 0.52
rs599839 1 SORT1 A 1.17 (1.11, 1.22) 0.78 0.78
rs3008621 1 MIA3 G 1.11 (1.04, 1.19) 0.26 NA
rs501120 10 Unknown T 1.30 (1.12, 1.51) 0.84 0.87
rs9818870 3 MRAS T 1.15 (1.11, 1.19) 0.15 0.15
rs3184504 12 SH2B3 T 1.13 (1.08, 1.18) 0.39 0.49
rs9982601 21 MRPS6 T 1.20 (1.14, 1.27) 0.13 0.14
rs12526453 6 PHACTR1 C 1.12 (1.08, 1.17) 0.65 0.67
rs6725887 2 WDR12 C 1.17 (1.11, 1.23) 0.14 0.13
rs1122608 19 LDLR G 1.15 (1.10, 1.21) 0.75 0.77
rs11206510 1 PCSK9 T 1.15 (1.10, 1.21) 0.81 0.82
rs1746048 10 CXCL12 C 1.16 (1.09, 1.24) 0.84 0.87