Skip to main content
. 2018 May 8;19:71. doi: 10.1186/s12881-018-0587-8

Table 3.

Top ranked SNPs associated with DME and PDR. SNPs with p < 1.0 × 10− 5 for each phenotype are shown

Phenotype Chr SNP Position in hg 38 (bp) Minor allele MAF cases MAF controls OR (95% CI) P Nearest gene
DME 2 rs1990145 75,650,524 A 0.364 0.268 2.02 (1.50, 2.72) 4.10 × 10− 6 MRPL19
13 rs4771506 105,843,651 C 0.325 0.263 1.97 (1.46, 2.64) 6.94 × 10− 6 LINC00343
PDR 5 rs918519 159,399,349 T 0.163 0.231 0.35 (0.22, 0.54) 3.87 × 10− 6 LOC285626
14 rs1158314 79,961,389 G 0.515 0.400 2.16 (1.56, 3.00) 4.01 × 10− 6 NRXN3
14 rs8004963 79,958,817 C 0.515 0.400 2.16 (1.56, 3.00) 4.01 × 10− 6 NRXN3
14 rs11159428 79,950,890 T 0.512 0.399 2.13 (1.54, 2.95) 5.63 × 10−6 NRXN3
5 rs918520 159,399,302 C 0.131 0.211 0.34 (0.21, 0.54) 6.66 × 10− 6 LOC285626

Odds ratios (OR) calculated with respect to the minor allele. P values are adjusted for age, duration of diabetes, sex, hypertension, nephropathy (defined as microalbuminuria or worse), HbA1c and the first 3 principal components. Chr chromosome, MAF minor allele frequency