Table 4.
Protective variants | Genotypes | TG1 |
---|---|---|
No (N = 916) | H+H+447SS (n = 916) | 1.17 (1.13 - 1.22) |
One (N = 519) | H+H-447SS (n = 459) | 1.11 (1.06 - 1.16) |
H-H-447SS (n = 56) | ||
H+H+447SX (n = 4) | ||
Two (N = 390) | H+H-447SX (n = 284) | 1.00 (0.95 - 1.06)2 |
H-H-447SX (n = 76) | ||
H-H-447XX (n = 30) |
H+ represents the most frequent allele of the HindIII variant and H- the least frequent allele. 1Geometric means (mmol/L) and 95% confidence intervals. p < 0.0001 of ANOVA test. 2Significantly different as compared to groups carrying one or no protective variant.