Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population
Table 3
Allele association analysis with these SNPs.
SNP
XFS/XFG
Control
OR (95% CI)
TBC1D21
rs16958445
Allele
G
432
583
3.025
0.082
1.369 (0.960–1.953)
A
70
69
ATXN2
rs7137828
Allele
T
429
531
3.272
0.070
0.7467 (0.544–1.025)
C
73
121
APOE
rs429358
Allele
T
452
587
C
50
65
<0.001
0.996
0.999 (0.677–1.473)
rs7412
Allele
C
468
610
T
34
42
0.051
0.822
1.055 (0.661–1.685)
CLU
rs2279590
Allele
C
351
455
T
151
197
0.002
0.961
0.994 (0.771–1.280)
AFAP1
rs11732100
Allele
C
402
524
T
100
128
0.015
0.903
1.018 (0.760–1.364)
TXNRD2
rs35934224
Allele
C
446
574
T
56
78
0.180
0.671
0.924 (0.642–1.331)
CACNA1A
rs4926244
Allele
T
401
515
C
101
137
0.138
0.710
0.947 (0.710–1.263)
ABCA1
rs2472493
Allele
A
301
391
G
201
261
<0.001
0.998
1.000 (0.789–1.269)
LOXL1
rs41435250
Allele
G
379
552
T
123
100
15.280
<0.001
1.791 (1.334–2.405)
rs893818
Allele
G
418
442
A
84
210
35.780
<0.001
0.423 (0.318–0.563)
GAS7
rs9897123
Allele
C
249
341
T
253
311
0.827
0.363
1.114 (0.883–1.406)
CNTNAP2
rs2107856
Allele
G
299
390
T
203
262
0.008
0.930
1.011 (0.797–1.281)
rs2141388
Allele
C
301
391
T
201
261
<0.001
0.998
1.000 (0.789–1.269)
G allele of rs41435250 of LOXL1 was the risk allele for the disorder. In contrast, G allele of rs893818 of LOXL1 was the protective allele for the disorder. Other alleles of SNPs showed no statistical significance.