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. 2018 Oct 25;11:391. doi: 10.3389/fnmol.2018.00391

Table 2.

Meta-analysis of the risk alleles of SNCA in each group.

Variants Alleles and related data In total East Asian European Mixed* Latino West Asian*
rs181489 T OR (95%CI) 1.28 [1.17, 1.40] 1.27 [1.15, 1.39]
p-value <0.00001 <0.00001
AF (P) 0.3486 0.3479 0.359
AF (C) 0.2974 0.299 0.2792
AF (G) 0.2531 0.0006 0.3071 0.1866
rs356165 G OR (95%CI) 1.25 [1.15, 1.37] 1.14 [0.97, 1.34] 1.37 [1.25, 1.50]
p-value <0.00001 0.11 <0.00001
AF (P) 0.5117 0.5982 0.4098 0.4512
AF (C) 0.4631 0.5489 0.3399 0.3979
AF (G) 0.4601 0.5293 0.3654 0.4688
rs356186 A OR (95%CI) 0.77 [0.70, 0.86] 0.77 [0.70, 0.86]
p-value <0.00001 <0.00001
AF (P) 0.1629 0.1629
AF (C) 0.2008 0.2008
AF (G) 0.194 0.1559 0.2 0.244
rs356219 G OR (95%CI) 1.30 [1.23, 1.38] 1.39 [1.15, 1.68] 1.26 [1.19, 1.34]
p-value <0.00001 0.0007 <0.00001
AF (P) 0.4723 0.6356 0.4367 0.452 0.6058
AF (C) 0.4038 0.555 0.3776 0.3483 0.4745
AF (G) 0.4549 0.5276 0.3654 0.4677
rs356220 T OR (95%CI) 1.23 [1.14, 1.33]
p-value <0.00001
AF (P) 0.4865 0.5907 0.4181 0.4154
AF (C) 0.4363 0.5543 0.3715 0.3442
AF (G) 0.4543 0.5224 0.3608 0.4513
rs356221 A OR (95%CI) 1.15 [0.94, 1.40] 1.15 [0.85, 1.55]
p-value 0.16 0.37
AF (P) 0.6257 0.664 0.4879
AF (C) 0.5963 0.628 0.459
AF (G) 0.5591 0.605 0.4584 0.5252
rs894278 G OR (95%CI) 1.13 [0.87, 1.46] 1.13 [0.87, 1.46]
p-value 0.37 0.37
AF (P) 0.3926 0.3926
AF (C) 0.3626 0.3626
AF (G) 0.1479 0.368 0.0482 0.1878
rs2301134 A OR (95%CI) 1.00 [0.74, 1.34]
p-value 0.97
AF (P) 0.2559 0.1245 0.5312
AF (C) 0.2454 0.1301 0.5066
AF (G) 0.4248 0.1582 0.4935 0.4079
rs2301135 G OR (95%CI) 1.24 [0.87, 1.76] 1.07 [0.98, 1.17]
p-value 0.23 0.13
AF (P) 0.3559 0.0873 0.5188
AF (C) 0.3581 0.0799 0.502
AF (G) 0.4179 0.1591 0.4944 0.406
rs2583988 T OR (95%CI) 1.21 [1.08, 1.35] 1.16 [1.04, 1.31]
p-value 0.001 0.009
AF (P) 0.2981 0.2968 0.2885
AF (C) 0.2648 0.2682 0.1939
AF (G) 0.1982 0.1495 0.2676 0.1495
rs2619363 T OR (95%CI) 1.13 [1.02, 1.24] 1.13 [1.02, 1.24]
p-value 0.01 0.01
AF (P) 0.3051 0.3051
AF (C) 0.2802 0.2802
AF (G) 0.1887 0.0006 0.2674 0.1504
rs2619364 G OR (95%CI) 1.24 [1.11, 1.40] 1.24 [1.11, 1.40]
p-value 0.0003 0.0003
AF (P) 0.302 0.302
AF (C) 0.2587 0.2587
AF (G) 0.1891 0.0006 0.2676 0.1495
rs2736990 G OR (95%CI) 1.22 [1.13, 1.31] 1.22 [1.11, 1.35]
p-value <0.00001 <0.0001
AF (P) 0.6092 0.6618 0.5101 0.6587
AF (C) 0.5602 0.6191 0.47 0.5255
AF (G) 0.554 0.6117 0.457 0.524
rs2737029 G OR (95%CI) 1.38 [1.20, 1.59] 1.30 [1.16, 1.45]
p-value <0.00001 <0.00001
AF (P) 0.5205 0.6842 0.4451
AF (C) 0.4478 0.5756 0.3839
AF (G) 0.4505 0.5437 0.3903
rs7684318 C OR (95%CI) 1.53 [1.22, 1.91] 1.53 [1.22, 1.91]
p-value 0.0003 0.0003
AF (P) 0.5913 0.5913
AF (C) 0.5229 0.5229
AF (G) 0.1912 0.5318 0.057 0.2818
rs11931074 T OR (95%CI) 1.36 [1.29, 1.44] 1.34 [1.26, 1.44] 1.37 [1.24, 1.52]
p-value <0.00001 <0.00001 <0.00001
AF (P) 0.2825 0.6023 0.0917 0.1008 0.2932 0.325
AF (C) 0.2501 0.5297 0.069 0.076 0.2296 0.2404
AF (G) 0.2344 0.5281 0.0623 0.2936

The bold characters and numbers represent the most recommended variants and corresponding relevant data (p < 1 × 10−5).

AF, allele frequency; P, patients; C, controls; G, GnomAD database; OR, odds ratio; CI, confidence interval;

*

no related AF in the GnomAD database.