Fig. 1
From: Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population
CHD Incidence by genotype for six MEOX2 SNPs (Panels a-f). Estimates were standardised to the mean of the distributions of sex and age in the whole study population. Vertical bars denote the standard error. P-values refer to the difference between minor allele carriers and major allele homozygotes. Cumulative incidence did not differ between minor allele homozygotes and heterozygotes (0.23 ≤ P ≤ 0.98 [a, c-f]), except for rs12056299 (P = 0.014 [b]). Median follow-up was 15.2 years. Tabulated data are the number of participants at risk by genotype at 6-year intervals