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Table 3 Genome-wide significant T2D-ESKD associations (P < 5 × 10−8) in baseline model

From: Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

Lead variant

CHR

POS

Locus

Effect/other alleles

Stage 1a (1513 T2D-ESKD cases vs. 5299 non-diabetic non-nephropathy controls)

Stage 1b (1700 T2D-ESKD cases vs. 770 non-diabetic non-nephropathy controls)

Stage 1c (219 T2D-ESKD cases vs. 908 non-diabetic non-nephropathy controls)

Stage 2: Meta-analysis (3432 T2D-ESKD cases vs. 6977 non-diabetic non-nephropathy controls)

EAF

OR (95% CI)

P

Info

EAF

OR (95% CI)

P

Info

EAF

OR (95% CI)

P

Info

EAF

OR (95% CI)

P

HetP

rs72858591

2

151711452

RND3/RBM43

C/T

0.10

1.55 (1.33,1.8)

1.32E−08

0.96

0.09

1.19 (0.92,1.54)

0.18

0.98

0.10

1.14 (0.72,1.82)

0.57

0.97

0.10

1.43 (1.26,1.62)

4.54E−08

0.15

rs58627064

3

165051826

SLITRK3

T/G

0.07

1.84 (1.53,2.2)

4.38E−11

0.91

0.06

1.19 (0.87,1.64)

0.27

0.97

0.06

1.25 (0.7,2.23)

0.46

1.00

0.06

1.62 (1.39,1.89)

6.81E−10

0.045

rs142563193

17

77667171

ENPP7

A/G

0.22

0.69 (0.6,0.78)

3.27E−08

0.64

0.23

0.81 (0.68,0.96)

0.018

0.97

0.25

0.91 (0.66,1.26)

0.57

0.97

0.23

0.74 (0.67,0.82)

1.24E−08

0.15

rs142671759

17

77706698

ENPP7

C/T

0.03

2.82 (2.05,3.87)

1.53E−10

0.73

0.02

1.15 (0.62,2.12)

0.66

0.82

0.02

1.53 (0.57,4.13)

0.40

0.92

0.02

2.26 (1.72,2.97)

5.53E−09

0.029

rs4807299

19

2570002

GNG7

A/C

0.05

1.95 (1.58,2.41)

7.31E−10

0.79

0.04

1.12 (0.76,1.65)

0.56

0.88

0.05

1.16 (0.58,2.32)

0.68

0.92

0.05

1.67 (1.4,2)

3.21E−08

0.028

rs9622363

22

36656555

APOL1

A/G

0.46

0.78 (0.7,0.85)

2.55E−07

0.87

0.44

0.77 (0.66,0.89)

0.00040

1.00

0.48

0.77 (0.58,1.03)

0.08

0.97

0.45

0.77 (0.72,0.84)

1.42E−10

0.995

  1. Baseline model: adjusted for age, sex, and PC1, APOL1 risk genotype carriers were included
  2. 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