Table 6.
Lead variant | CHR | POS | Locus | Effect/other allele | *Info | Stage 2: Meta-analysis (2768 T2D-ESKD cases vs. 6059 non-diabetic non-nephropathy controls) | Stage 4 (1019 non-diabetic ESKD cases vs. 733 non-diabetic non-nephropathy controls) | Stage 5 (3787 all-cause ESKD cases vs. 6059 non-diabetic non-nephropathy controls) | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
EAF | OR (95% CI) | P | EAF | OR(95% CI) | P | EAF | OR (95% CI) | P | HetP | ||||||
rs12472637 | 2 | 30304514 | ALK/YPEL5 | A/G | 0.94 | 0.33 | 0.81 (0.74, 0.89) | 6.05E−06 | 0.36 | 0.8 (0.66, 0.96) | 0.019 | 0.33 | 0.82 (0.76, 0.89) | 4.47E−06 | 0.83 |
rs76971802 | 3 | 188607071 | LPP | T/C | 0.95 | 0.09 | 1.43 (1.24, 1.65) | 1.06E−06 | 0.08 | 1.45 (1.03, 2.05) | 0.032 | 0.088 | 1.42 (1.24, 1.62) | 5.76E−07 | 0.93 |
rs6459733 | 7 | 156930550 | MNX1-AS1/UBE3C | G/C | 0.97 | 0.39 | 1.25 (1.15, 0.87) | 1.32E−07 | 0.39 | 1.25 (1.03, 1.53) | 0.026 | 0.39 | 1.24 (1.15, 1.35) | 7.17E−08 | 0.83 |
rs4910809 | 11 | 3813850 | NUP98 | C/G | 0.98 | 0.02 | 0.53 (0.4, 0.7) | 9.46E−06 | 0.02 | 0.53 (0.29, 0.95) | 0.034 | 0.023 | 0.53 (0.41, 0.69) | 2.12E−06 | 0.63 |
rs219020 | 13 | 63013622 | LINC01075/LINC00448 | C/T | 0.97 | 0.14 | 1.31 (1.17, 0.86) | 6.84E−06 | 0.11 | 1.38 (1.02, 1.87) | 0.037 | 0.14 | 1.31 (1.17, 1.47) | 2.12E−06 | 0.58 |
rs113452507 | 15 | 37954309 | TMCO5A | C/G | 0.92 | 0.16 | 1.29 (1.15, 1.45) | 9.71E−06 | 0.16 | 1.38 (1.07, 1.77) | 0.014 | 0.16 | 1.31 (1.18, 1.45) | 8.48E−07 | 0.93 |
rs373971520 | 19 | 2568805 | GNG7 | –/CA | 0.81 | 0.11 | 1.47 (1.28, 1.7) | 8.97E−08 | 0.11 | 1.39 (1.01, 1.91) | 0.044 | 0.11 | 1.46 (1.28, 1.67) | 2.17E−08 | 0.016 |
rs6094913 | 20 | 46561443 | SULF2/LINC01522 | G/A | 0.93 | 0.09 | 0.72 (0.63, 1.6) | 8.28E−06 | 0.10 | 0.67 (0.48, 0.91) | 0.012 | 0.092 | 0.72 (0.63, 0.83) | 2.5E−06 | 0.70 |
Abbreviations: T2D type 2 diabetes, ESKD end-stage kidney disease, CHR chromosome, POS position, EAF effect allele frequency, OR odds ratio, CI confidence interval, P P value, *Info imputation quality, HetP heterogeneity P value;
APOL1-negative model: adjusted for age, sex, and PC1; APOL1 risk genotype carriers were excluded