Table 2.
Phenotype; bin | Chromosomal location | Average rank |
P-value for low heterogeneity | |
Observed | P-value | |||
eGFR | ||||
9.1 | 9p24.3–9p22.3 | 84 | 0.0052 | 0.4145 |
7.2 | 7p15.3–7p13 | 83 | 0.0062 | 0.6830 |
16.3 | 16q12.2–16q23.1 | 82 | 0.0072 | 0.5705 |
13.4 | 13q33.1–13q34 | 78 | 0.0250 | 0.6052 |
14.3 | 14q23.3–14q32.12 | 77 | 0.0298 | 0.5067 |
7.4 | 7q11.23–7q22.3 | 76 | 0.0401 | 0.2298 |
Serum creatinine | ||||
9.6 | 9q34.11–9q34.3 | 88 | 0.0017 | 0.4266 |
7.3 | 7p13–7q11.23 | 86 | 0.0029 | 0.8663 |
16.4 | 16q23.1–16q24.1 | 81 | 0.0119 | 0.8982 |
9.4 | 9q21.32–9q31.2 | 80 | 0.0151 | 0.7710 |
10.3 | 10p11.23–10q22.1 | 79 | 0.0185 | 0.5645 |
9.5 | 9q31.2–9q34.11 | 78 | 0.0278 | 0.4132 |
9.2 | 9p22.3–9p21.1 | 78 | 0.0306 | 0.9721 |
9.3 | 9p21.1–9q21.32 | 78 | 0.0308 | 0.9793 |
11.4 | 11q13.3–11q22.1 | 77 | 0.0376 | 0.8685 |
11.3 | 11p12–11q13.3 | 76 | 0.0452 | 0.7713 |
Creatinine clearance | ||||
7.3 | 7p13–7q11.23 | 93 | 0.0195 | 0.6463 |
6.6 | 6q25.3–6q27 | 91 | 0.0310 | 0.5524 |
16.4 | 16q23.1–16q24.1 | 91 | 0.0315 | 0.6064 |
10.4 | 10q22.1–10q23.32 | 90 | 0.0337 | 0.9859 |
2.6 | 2q21.1–2q24.1 | 88 | 0.0409 | 0.7208 |
ACR | ||||
10.4 | 10q22.1–10q23.32 | 82 | 0.0145 | 0.9425 |
7.5 | 7q22.3–7q34 | 82 | 0.0154 | 0.3294 |
3.6 | 3q21.2–3q25.32 | 81 | 0.0190 | 0.3643 |
7.4 | 7q11.23–7q22.3 | 81 | 0.0205 | 0.5862 |
1.2 | 1p36.21–1p35.2 | 79 | 0.0305 | 0.1693 |
GFR, glomerular filtration rate. The threshold for genome-wide significance would be P-value ≤0.05/120 = 0.00042. No bin attained this level in the main analysis.