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. 2020 Jul 30;15(7):e0236071. doi: 10.1371/journal.pone.0236071

Table 3. Comparison of the genotype frequencies between the HM vs. No HM group.

Cohort 1 Cohort 2
SNPs Genotype Control Genotype frec (%) Genotype cases (n) HM Genotype frec (%) Genotype cases (n) Genot. Uncor. p-value Control Genotype frec (%) Genotype cases (n) HM Genotype frec (%) Genotype cases (n) Genot. Uncor. p-value Control Genotype frec (%) Genotype cases (n) HM Genotype frec (%) Genotype cases (n) Genotype Uncorrected p-value Genotype OR (95% CI)
rs11873429 AA/AC/CC 91.3/8.7/0 63/3/0 93.4/6.0/0.6 157/10/1 0.79 94.6/5.4/0 35/2/0 95.2/4.8/0 79/4/0 0.76 92.5/7.5/0 98/8/0 94/5.6/0.4 235/14/1 C; 0.63 0.80 (0.3–2.1)
rs577948 AA/AG/GG 34.4/48.7/17.2 22/31/11 29.8/51.6/18.6 48/83/30 0.71 26.9/34.6/38.5 7/9/10 33.3/43.2/23.5 27/35/19 0.53 32.2/44.4/23.3 29/40/21 31/48.8/20.2 75/118/49 C; 0.62 1.24 (0.7–2.3)
rs669676 AA/AG/GG 35.4/45.6/19 28/36/15 29.3/44.2/26.5 63/95/57 0.27 33.3/56.7/10 10/17/3 30.7/46.5/22.8 31/47/23 0.22 34.9/48.6/16.5 38/53/18 29.3/45.2/25.5 92/142/80 R; 0.08 1.65 (0.9–3.0)
rs13095226 CC/CT/TT 83.8/16.2/0 62/12/0 82.3/15.8/1.9 177/34/4 0.24 93.5/6.5/0 29/2/0 73/23.4/3.6 81/26/4 0.13 86.7/13.3/0 91/14/0 79.3/18.6/2.1 256/60/7 R; 0.07 NA (0.0-NA)
rS644242 AA/AC/CC 87.6/12.4/0 78/11/0 93.5/5.6/0.9 101/6/1 0.37 90/10/0 27/3/0 90.1/9.9/0 100/11/0 0.6 88.2/11.8/0 105/14/0 91.8/7.8/0.4 201/17/1 C; 0.64 0.68 (0.3–1.6)
rs634990 CC/CT/TT 30.3/46.1/23.6 27/41/21 29.5/49.3/21.2 64/107/46 0.40 13.3/53.3/33.3 4/16/10 39.6/37.8/22.5 44/42/25 0.017 26.1/47.9/26.1 31/57/31 33.1/45.4/21.5 108/148/70 D; 0.43 0.71 (0.4–1.2)
rs74315511 CC/CT/TT 89 213 - 30 110 - 119 322 - -
rs8139305 AA/AG/GG 88 213 - 29 110 - 117 322 - -

Chr: Chromosome; Genotype freq: Genotype frequency; OR: Odds ratio; CI: Confidence interval; P-value: value from logistic regression model; P value significance < 0.05. C; Codominant model (XX vs XY vs YY), R; Recessive model (XX-XY vs YY) D; Dominant model (XX vs XY-YY).