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. 2010 Oct 23;376(9750):1393–1400. doi: 10.1016/S0140-6736(10)61267-6

Table 2.

Association between SNPs and incident coronary heart disease, cardiovascular disease, and myocardial infarction*

Region Candidate gene(s) Weight Reference Risk allele Risk allele frequency Other allele Coronary heart disease (total n=19 790)
Cardiovascular disease (total n=24 894)
Myocardial infarction (total n=24 894)
Pooled HR (95% CI) p value Pooled HR (95% CI) p value Pooled HR (95% CI) p value
rs17465637 1q41 MIA3 1·14 15 C 0·75 A 0·99 (0·87–1·12) 0·854 1·03 (0·94–1·12) 0·546 1·03 (0·91–1·18) 0·624
rs11206510 1p32 PCSK9 1·15 15 T 0·84 C 0·94 (0·81–1·09) 0·431 0·97 (0·87–1·07) 0·515 1·04 (0·89–1·22) 0·636
rs646776 1p13 CELSR2–PSRC1–SORT1 1·19 15 T 0·79 C 0·96 (0·84–1·09) 0·512 0·98 (0·89–1·07) 0·587 0·94 (0·82–1·08) 0·378
rs6725887 2q33 WDR12 1·17 15 C 0·11 T 1·14 (0·96–1·35) 0·126 1·00 (0·89–1·12) 0·960 0·96 (0·80–1·14) 0·629
rs9818870 3q22 MRAS 1·15 16 T 0·10 C 0·88 (0·73–1·06) 0·174 0·92 (0·81–1·03) 0·150 0·86 (0·71–1·03) 0·097
rs3798220 6q26 LPA 1·68 18 C 0·01 T 2·07 (1·39–3·09) 3·8×10−5 1·63 (1·22–2·17) 0·001 1·80 (1·19–2·72) 0·005
rs9349379 6p24 PHACTR1 1·12 15 C 0·44 T 1·16 (1·04–1·29) 0·008 1·10 (1·02–1·19) 0·014 1·11 (0·99–1·24) 0·075
rs4977574 9p21 CDKN2A–CDKN2B 1·29 15 G 0·43 A 1·21 (1·08–1·34) 0·001 1·16 (1·08–1·25) 9·3×10−6 1·19 (1·06–1·33) 0·002
rs1746048 10q11 CXCL12 1·17 15 C 0·84 T 1·13 (0·97–1·33) 0·113 1·01 (0·91–1·12) 0·846 1·11 (0·95–1·31) 0·198
rs2259816 12q24 HNF1A 1·08 16 T 0·36 G 1·02 (0·91–1·14) 0·774 1·00 (0·92–1·08) 0·932 1·01 (0·90–1·14) 0·836
rs3184504 12q24 SH2B3 1·13 17 T 0·40 C 1·03 (0·92–1·15) 0·568 1·10 (1·02–1·19) 0·011 1·15 (1·03–1·29) 0·012
rs1122608 19p13 LDLR 1·15 15 G 0·79 T 1·00 (0·87–1·14) 0·988 1·02 (0·93–1·12) 0·693 0·98 (0·86–1·12) 0·774
rs9982601 21q22 SLC5A3–MRPS6–KCNE2 1·20 15 T 0·14 C 1·29 (1·07–1·57) 0·009 1·11 (0·98–1·26) 0·092 1·24 (1·04–1·48) 0·016

SNP=single nucleotide polymorphism. HR=hazard ratio.

*

Association tested with Cox proportional hazards model adjusted for sex, LDL and HDL cholesterol, smoking, body-mass index, systolic and diastolic blood pressure, blood pressure treatment, and diabetes; age was used as the timescale.

SNP specific weights for genetic risk score calculation; weights are effect sizes for the SNPs from the studies referenced.

Results from FINRISK 1992, 1997, and 2002, Health 2000, and Malmö Diet and Cancer Cardiovascular Cohort were combined with fixed effects meta-analysis.21