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. 2018 May 14;41(2):403–409. doi: 10.1590/1678-4685-GMB-2017-0147

Table 2. Allele and genotype distribution and frequencies of the ARNTL, CLOCK, CRY2 and PER2 polymorphisms.

Gene SNP Minor allele MAF* patients MAF* controls p-value Genotype Genotype frequency (%)
Patients with MI Controls p-value X2 q value
ARNTL1 rs3789327 C 0.42 0.44 0.475 CC 33.5 34.0 0.301 2.34 0.443
CT 50.0 44.0
TT 16.5 22.0
rs4757144 A 0.62 0.59 0.385 AA 39.5 36.0 0.694 0.73 0.867
AG 45.5 46.5
GG 15.0 17.5
rs12363415 G 0.15 0.17 0.501 AA 71.0 71.0 0.120 4.24 0.300
AG 27.5 24.0
GG 1.5 5.0
CLOCK rs11932595 G 0.39 0.39 0.942 AA 36.5 35.0 0.878 0.26 0.878
AG 49.5 52.0
GG 14.0 13.0
rs6811520 T 0.39 0.49 0.004 CC 37.5 31.0 0.005 10.55 0.050
CT 47.0 40.0
TT 15.5 29.0
rs13124436 A 0.33 0.28 0.143 AA 11.0 7.0 0.294 2.45 0.443
AG 43.0 41.5
GG 46.0 51.5
CRY2 rs2292912 G 0.20 0.26 0.054 CC 62.0 55.5 0.056 5.78 0.197
CG 35.5 37.0
GG 2.5 7.5
rs10838524 A 0.45 0.49 0.230 AA 19.0 26.3 0.212 3.11 0.424
AG 52.5 46.5
GG 28.5 27.2
PER2 rs35333999 T 0.05 0.09 0.032 CC 91.5 84.0 0.059 5.64 0.197
CT 7.5 15.0
TT 1.0 1.0
rs934945 T 0.17 0.19 0.644 CC 69.0 67.5 0.864 0.29 0.878
CT 27.5 28.0
TT 3.5 4.5
*

MAF –minor allele frequency

Pearson Chi-square test

CLOCK SNP rs6811520 showed a departure from the Hardy-Weinberg equilibrium and was excluded

p-values shown in the table are corrected for the multiple comparisons.