Research Article

IL-9 and IL-10 Single-Nucleotide Variants and Serum Levels in Age-Related Macular Degeneration in the Caucasian Population

Table 7

Haplotype association with the predisposition to AMD occurrence.

SNP1SNP2SNP3SNP4SNP5SNP6SNP7SNP8FrequencyOR (95% CI) value

Haplotype associations with early AMD
1GACGG0.77151
2AGTAT0.14680.76 (0.54-1.08)0.13
3AGCGG0.03350.49 (0.25-0.95)0.035
4AATAT0.0181.74 (0.72-4.22)0.22
5GATAT0.01080.08 (0.01-0.61)0.015
6AACGG0.01032.25 (0.66-7.66)0.19
7 (rare)0.0091.29 (0.32-5.21)0.72
8GGC0.45491
9GGT0.32751.13 (0.89-1.44)0.31
10ATT0.21661.00 (0.75-1.32)0.98
11 (rare)0.001<0.001 (-)1

Haplotype associations with exudative AMD
1GACGG0.77131
2AGTAT0.14870.96 (0.69-1.35)0.83
3AGCGG0.04080.99 (0.57-1.73)0.98
4AATAT0.01651.11 (0.46-2.66)0.82
5 (rare)0.02270.37 (0.15-0.92)0.033
6GGC0.47511
7GGT0.30260.87 (0.68-1.10)0.24
8ATT0.22050.94 (0.72-1.22)0.63
9 (rare)0.00180.34 (0.02-5.66)0.45

Haplotype associations with atrophic AMD
1GACGG0.75581
2AGTAT0.15181.25 (0.65-2.40)0.5
3AGCGG0.04532.34 (0.93-5.88)0.071
4GATAT0.0167<0.00 (-)1
5AATAT0.01621.05 (0.23-4.68)0.95
6 (rare)0.01420.55 (0.07-4.43)0.57
7GGC0.47581
8GGT0.30460.62 (0.38-1.02)0.06
9ATT0.2180.78 (0.47-1.29)0.33
10 (rare)0.0016<0.00 (-)1

Rare: pooled rare haplotypes; OR: odds ratio; CI: confidence interval; p: significance level when ; SNP1: rs1859430; SNP2: rs2069870; SNP3: rs11741137; SNP4: rs2069885; SNP5: rs2069884; SNP6: rs1800871; SNP7: rs1800872; SNP8: rs1800896.