Table 2 Location and allele frequencies of sequence variation identified in PDS/PG cases and controls
From: Common sequence variants in the LOXL1gene in pigment dispersion syndrome and pigmentary glaucoma
Position | SNP | Variation | PDS*/PG† | Controls | P |
|---|---|---|---|---|---|
Exon 1 | rs1048661 | G/T | G = 0.66 | G = 0.71 | NS‡ |
T = 0.34 | T = 0.29 | ||||
Exon 1 | rs3825942 | G/A | G = 0.84 | G = 0.8 | NS |
A = 0.16 | A = 0.2 | ||||
Exon 1 | rs2165241 | C/T | C = 0.51 | C = 0.50 | NS |
T = 0.49 | T = 0.50 | ||||
Intron 5 | rs2304722 | C/T | C = 0.09 | C = 0.21 | 1.62e-4 |
T = 0.91 | T = 0.79 | ||||
Exon 7 | rs8818 | G/C | G = 0.69 | G = 0.68 | NS |
C = 0.31 | C = 0.32 | ||||
Exon 7 | rs3522 | C/T | T = 0.44 | T = 0.45 | NS |
C = 0.56 | C = 0.55 |