Table 2 of Fuse, Mol Vis 2008; 14:1338-1343.


Table 2. Frequency of genotypes, p.R141L, p. G153D, and rs2165241, of LOXL1 in patients with XFS, XFG, and control subjects.


Genotype
XFS all
(n=56)
XFG
(n=36)
XFS no
glaucoma (n=20)
POAG
(n=62)
Control
(n=138)
LOXL1 p.R141L (rs1048661) variant
T/T 53 (94.6%) 34 (94.4%) 19 (95.0%) 23 (37.1%) 30 (21.7%)
T/G 2 (3.6%) 1 (2.8%) 1 (5.0%) 29 (46.8%) 80 (58.0%)
G/G 1 (1.8%) 1 (2.8%) 0 10 (16.1%) 28 (20.3%)
p value* 1.6x10−19 7.8x10−15 3.0x10−10 0.15
LOXL1 p.G153D (rs3825942) variant
G/G 56 (100%) 36 (100%) 20 (100%) 51 (82.3%) 108 (78.3%)
G/A 0 0 0 11 (17.7%) 26 (18.8%)
A/A 0 0 0 0 4 (2.9%)
p value* 7.5x10−4 8.8x10−3 0.068 0.58
LOXL1rs2165241 variant
C/C 54(96,4%) 34(94.4%) 20(100%) 56(91.3%) 122(88.4%)
C/T 2(3.6%) 2(5.6%) 0 6(9.7%) 16(11.6%)
T/T 0 0 0 0 0
p value* 0.08 0.29 0.11 0.69