Table 2.
Polymorphism2 | rs number | Position5 |
Minor allele frequency |
OR (95% CI) | P Value | |
Patients (n = 195) | Controls (n = 150) | |||||
G-974C4 | rs283887 | 79200522 | 0.01 | 0.02 | 0.49 (0.02-7.10) | 1.001 |
G-938A | rs1349077 | 79200558 | 0.34 | 0.33 | 1.05 (0.56-1.96) | 0.88 |
T-912G | rs283888 | 79200584 | 0.49 | 0.50 | 0.94 (0.54-1.78) | 0.84 |
G-501A4 | rs283889 | 79200995 | 0.01 | 0.02 | 0.49 (0.02-7.10) | 1.001 |
T-385C | rs10165462 | 79201111 | 0.32 | 0.29 | 1.15 (0.60-2.20) | 0.65 |
-331delGGA3 | - | - | 0.01 | 0.01 | 1.00 | 1.001 |
T-243G | rs283890 | 79201253 | 0.34 | 0.35 | 1.09 (0.75-1.58) | 0.63 |
G209T | rs2070707 | 79201704 | 0.20 | 0.17 | 1.29 (0.78-2.12) | 0.29 |
G2199A | rs3739142 | 79203694 | 0.34 | 0.34 | 1.01 (0.70-1.48) | 0.94 |
G2370A34 | - | - | 0.01 | 0.03 | 0.33 (0.01-3.60) | 0.611 |
AA: Amino acid; OR: Odds ratio; CI: Confidence interval;
Yates corrected P value;
Nomenclature as per NCBI sequence Accession No. NT_022184;
Novel polymorphism;
Data from 50 patients & 50 controls;
Chromosomal location according to UCSC Genome Browser, March 2006 build (dbSNP build 126).