Table 2.
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) |
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---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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