Table 2. Frequencies of CCL5 genotypes in the subcohort and hazard ratios (HR) and 95% confidence intervals (CI) for incident coronary events comparing CCL5 genotypes in the case-cohort dataset (MONICA/KORA Augsburg case-cohort study).
SNP | Allele* | n* | Weighted frequency (%)* | Model** | HR (95% CI) for genotype* | ||
1/2 | 11/12/22 | 11/12/22 | 11 | 12 | 22 | ||
rs2107538 | C/T | 1382/661/76 | 65.2/31.2/3.6 | 1 | 1 (ref) | 1.06 (0.81–1.37) | 0.98 (0.52–1.84) |
2 | 1 (ref) | 1.04 (0.79–1.37) | 1.13 (0.61–2.09) | ||||
rs2280788 | C/G | 2036/90/0 | 95.8/4.2/0 | 1 | 1 (ref) | 0.55 (0.26–1.13) | N/A |
2 | 1 (ref) | 0.57 (0.26–1.23) | N/A | ||||
rs2280789 | T/C | 1601/488/40 | 75.2/22.9/1.9 | 1 | 1 (ref) | 1.01 (0.76–1.33) | 0.80 (0.30–2.11) |
2 | 1 (ref) | 0.99 (0.73–1.33) | 0.96 (0.39–2.40) | ||||
rs4796120 | A/G | 1691/414/30 | 79.2/19.4/1.4 | 1 | 1 (ref) | 1.02 (0.68–1.53) | 0.96 (0.29–3.15) |
2 | 1 (ref) | 0.95 (0.61–1.48) | 0.96 (0.29–3.15) | ||||
rs3817655 | T/A | 1380/665/80 | 64.9/31.3/3.8 | 1 | 1 (ref) | 1.06 (0.81–1.37) | 0.83 (0.44–1.58) |
2 | 1 (ref) | 1.04 (0.79–1.37) | 0.81 (0.40–1.65) | ||||
rs1065341 | A/G | 1880/231/11 | 88.6/10.9/0.5 | 1 | 1 (ref) | 1.00 (0.74–1.34) | 1.08 (0.39–2.98) |
2 | 1 (ref) | 0.98 (0.72–1.34) | 1.28 (0.50–3.31) |
*Allele 1 denotes the major allele, allele 2 denotes the minor allele. All alleles are shown in forward orientation according to dbSNP BUILD 133.
**Model 1: adjusted for age, sex and survey; Model 2: Model 1+BMI, systolic blood pressure, ratio of total cholesterol / HDL cholesterol, smoking status, alcohol intake, physical activity, history of diabetes.
N/A, not applicable (no homozygous carriers of the minor allele); ref, reference genotype.