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. 2020 Oct 23;11:590365. doi: 10.3389/fgene.2020.590365

Table 2.

Association analysis of rs17016188 and rs7684892 with PD risk.

Variant Allele, n (%) OR (95% CI) p Genotype, n (%) p
rs17016188 T C TT CT CC
Control 669 (66.0) 345 (34.0) 223 (44.0) 223 (44.0) 61 (12.0)
PD 634 (61.8) 392 (38.2) 1.199 (1.001–1.437) 0.049 207 (40.4) 220 (42.9) 86 (16.8) 0.089
Male control 388 (67.6) 186 (32.4) 127 (44.3) 134 (46.7) 26 (9.1)
Male PD 313 (59.3) 215 (40.7) 1.433 (1.120–1.833) 0.004* 99 (37.5) 115 (43.6) 50 (18.9) 0.003*
Female control 281 (63.9) 159 (36.1) 96 (43.6) 89 (40.5) 35 (15.9)
Female PD 321 (64.5) 177 (35.5) 0.974 (0.746–1.273) 0.850 108 (43.4) 105 (42.2) 36 (14.5) 0.884
rs7684892 G A GG AG AA
Control 824 (81.3) 190 (18.7) 335 (66.1) 154 (30.4) 18 (3.6)
PD 798 (77.8) 228 (22.2) 1.239 (0.999–1.537) 0.051 312 (60.8) 174 (33.9) 27 (5.3) 0.149
Male control 474 (82.6) 100 (17.4) 196 (68.3) 82 (28.6) 9 (3.1)
Male PD 409 (77.5) 119 (22.5) 1.379 (1.025–1.856) 0.033 163 (61.7) 83 (31.4) 18 (6.8) 0.079
Female control 350 (79.6) 90 (20.5) 139 (63.2) 72 (32.7) 9 (4.1)
Female PD 389 (78.1) 109 (21.9) 1.090 (0.796–1.492) 0.592 149 (59.8) 91 (36.8) 9 (3.6) 0.680

CI, confidence interval; OR, odds ratio; PD, Parkinson’s disease.

*

Indicates p < 0.025 after Bonferroni correction.