We found 126 genome-wide significant associations (P < 5 × 10−8, Supplementary Data 9), particularly for hypertension and blood counts: for 3 of the 11 variants, the eGFR-decreasing alleles were associated with increased risk of hypertension (near UMOD/PDILT, DCDC5, and PIK3CG). Here, DCDC1 is linked to hypertensive disorder.