Table 2 Results from cross-ancestry meta-analysis (chromosomes 8–22)

From: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

SNP

Chr:bp

Nearest gene

A1/A2

European-specific meta-analysis

Asian-specific meta-analysis

Cross-ancestry meta-analysis

A1F

β (SE)

P

A1F

β (SE)

P

A1F

β (SE)

P

N

rs3808520

8:23164773

LOXL2

c/g

0.21

2.50 (0.48)

2.61E-07

0.10

2.02 (0.88)

2.28E-02

0.18

2.39 (0.42)

2.02E-08

24,899

rs10429294

8:95969322

NDUFAF6

t/c

0.50

2.36 (0.39)

2.21E-09

0.66

1.34 (0.55)

1.60E-02

0.56

2.02 (0.32)

3.48E-10

24,899

rs7026684

9:4215308

GLIS3

a/g

0.36

−2.00 (0.39)

4.24E-07

0.39

−1.81 (0.55)

1.04E-03

0.37

−1.94 (0.32)

1.73E-09

25,910

rs66720556

9:13559717

MPDZ

a/t

0.18

−1.86 (0.51)

3.01E-04

0.25

−3.80 (0.59)

2.18E-10

0.21

−2.68 (0.39)

6.06E-12

24,071

rs10980623

9:113660537

LPAR1

a/g

0.79

−2.63 (0.46)

1.06E-08

0.79

−3.43 (0.63)

6.06E-08

0.79

−2.90 (0.37)

5.63E-15

25,910

rs3132303

9:137444298

COL5A1

c/g

0.26

5.23 (0.49)

6.11E-26

0.26

5.91 (0.71)

1.21E-16

0.26

5.45 (0.40)

8.35E-41

24,899

rs7040970

9:139859013

LCN12

t/c

0.49

3.35 (0.41)

3.54E-16

0.72

1.80 (0.63)

4.31E-03

0.56

2.89 (0.34)

4.75E-17

24,899

rs35809595

10:63831928

ARID5B

a/g

0.40

−2.29 (0.39)

8.97E-09

0.36

−2.66 (0.53)

6.56E-07

0.39

−2.43 (0.32)

3.40E-14

24,899

rs2419835

10:115296564

HABP2

t/c

0.86

2.21 (0.54)

4.70E-05

0.45

2.33 (0.52)

9.01E-06

0.65

2.27 (0.37)

1.74E-09

25,910

rs4938174

11:110913240

ARHGAP20-C11orf53

a/g

0.30

1.82 (0.41)

9.97E-06

0.15

3.74 (0.75)

6.14E-07

0.26

2.26 (0.36)

3.59E-10

25,910

rs56009602

11:130289612

ADAMTS8

t/c

0.05

6.86 (0.92)

1.30E-13

0.10

7.24 (0.93)

1.25E-14

0.08

7.05 (0.66)

1.16E-26

25,910

rs7308752

12:91527181

DCN

a/g

0.91

3.87 (0.67)

1.07E-08

0.73

2.28 (0.68)

7.91E-04

0.82

3.08 (0.48)

1.34E-10

25,302

rs11553764

12:104415244

GLT8D2

t/c

0.17

3.19 (0.53)

2.77E-09

0.20

4.14 (0.67)

8.62E-10

0.18

3.55 (0.42)

2.47E-17

24,899

rs10161679

13:23243645

FGF9-SGCG a

a/g

0.71

−2.40 (0.45)

1.41E-07

0.72

−1.99 (0.64)

2.16E-03

0.71

−2.26 (0.37)

1.28E-09

24,899

13:41112152

13:41112152

FOXO1

i/r

0.10

−5.44 (0.66)

2.15E-16

0.03

−2.52 (1.81)

1.64E-01

0.10

−5.10 (0.62)

2.54E-16

24,071

rs56223983

14:81814754

STON2

t/g

0.30

2.01 (0.42)

1.83E-06

0.30

1.99 (0.58)

5.94E-04

0.30

2.00 (0.34)

4.14E-09

25,910

rs785422

15:30173885

TJP1

t/c

0.11

−4.01 (0.63)

2.65E-10

0.08

−3.50 (1.26)

5.75E-03

0.10

−3.91 (0.56)

5.72E-12

21,810

rs8030753

15:48801935

FBN1

t/c

0.13

2.02 (0.55)

2.75E-04

0.27

2.51 (0.59)

2.29E-05

0.20

2.25 (0.40)

2.87E-08

25,910

rs12912010

15:67467143

SMAD3

t/g

0.22

2.76 (0.47)

6.40E-09

0.36

2.21 (0.53)

3.92E-05

0.28

2.52 (0.35)

1.50E-12

24,899

rs4843040

15:85838636

AKAP13 b

t/c

0.24

−2.92 (0.44)

3.62E-11

0.47

−2.35 (0.52)

6.68E-06

0.33

−2.68 (0.33)

1.68E-15

25,910

rs930847

15:101558562

LRRK1

t/g

0.77

−3.57 (0.45)

3.19E-15

0.73

−3.79 (0.61)

7.82E-10

0.76

−3.64 (0.36)

1.63E-23

25,910

rs35193497

16:88324821

ZNF469

t/g

0.36

−6.23 (0.43)

8.64E-47

0.29

−4.92 (0.62)

2.34E-15

0.34

−5.80 (0.35)

8.08E-60

24,899

rs4792535

17:14565130

HS3ST3B1

t/c

0.29

−2.43 (0.41)

3.61E-09

0.47

−2.04 (0.54)

1.72E-04

0.36

−2.29 (0.32)

3.13E-12

25,302

rs8133436

21:47519535

COL6A2

t/c

0.05

3.90 (1.07)

2.84E-04

0.25

3.47 (0.72)

1.85E-06

0.18

3.61 (0.60)

2.17E-09

24,899

rs71313931

22:19960184

ARVCF

c/g

0.71

−2.23 (0.44)

5.49E-07

0.78

−2.22 (0.70)

1.59E-03

0.73

−2.23 (0.37)

3.21E-09

24,071

  1. Nearest gene (reference NCBI build37) is given as locus label, but this should not be interpreted as providing support that the nearest gene is the best candidate, a list including all the genes +/− 200 kb of the lead SNP is presented in Supplementary Table 12
  2. New loci are in bold
  3. SNP rsID, Chr:bp chromosome: base pair, A1 risk allele, A2 other allele, A1F frequency of allele A1, β effect size on CCT based on allele A1, SE standard error of the effect size, i insertion, d deletion, r reference, N number of individuals included in the meta-analysis per variant
  4. aThe lead SNP is located 228KB 3′ of the pseudogene BASP1P1
  5. bThe lead SNP is located in pseudogene ADAMTS7P4