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. 2003 Sep;89(9):1023–1026. doi: 10.1136/heart.89.9.1023

Table 3.

Prevalence of the possible HFE genotypes in each subject group

Normal control (n=493) IHD control (n=427) MI survivor (n=828) Normal control v IHD control OR (95% CI) Normal control v MI survivor OR (95% CI)
Wild type 268 (54.4%) 249 (58.3%) 468 (56.5%) 1.17 (0.90 to 1.5) 1.14 (0.87 to 1.5)
H63D homozygote 10 (2.0%) 9 (2.1%) 23 (2.8%) 1.02 (0.41 to 2.6) 1.22 (0.51 to 2.9)
H63D heterozygote 115 (23.3%) 98 (23.0%) 198 (23.9%) 0.97 (0.71 to 1.3) 1.04 (0.76 to 1.4)
Compound heterozygote 15 (3.0%) 7 (1.6%) 31 (3.7%) 0.53 (0.21 to 1.3) 0.87 (0.42 to 1.8)
C282Y homozygote 5 (1.0%) 3 (0.7%) 7 (0.8%) 0.71 (0.17 to 3.0) 1.20 (0.23 to 6.2)
C282Y heterozygote 80 (16.2%) 61 (14.3%) 101 (12.2%) 0.88 (0.61 to 1.3) 0.70 (0.48 to 1.04)

None of the genotype groups achieved significance.

HFE, haemochromatosis gene.