Table 3 Association analysis of affective disorder and multiple related traits across the linkage regions in GS and UKB

From: DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

-LOG(P)

chr1q

chr11q1

chr11q2

chr5q

chr1p

chr2p

chr3q

chr4q

chr16p

GS_GWAS

3.39 CAPN8

3.84 GRM5

3.28 CNTN5

3.67 PDE4D

3.63 LRRC7

3.0 VSNL1

4.18 BCHE

3.32 GLRB

4.59 PRKCB

UKB_GWAS

3.18 TLR5

2.78 GRM5

3.82 CNTN5

3.92 PDE4D

3.68 LRRC7

4.05 VSNL1

4.16 EGFEM1P

5.2

5.09 TNRC6A

Neuroticism

2.05

1.96

3.08

2.91

2.17

2.06

3.10

2.77

3.21

Extroversion

2.45

2.60

2.29

5.22 PPWD1

2.73

2.07

2.33

2.22

2.77

Digit symbol coding

2.94

2.21

3.41 CNTN5

2.57

2.35

2.79

2.32

3.56 RAPGEF2

3.12

Verbal fluency

2.94

2.24

2.64

3.10

2.22

3.04

2.40

2.94

2.75

Vocabulary

3.01

2.43

3.49 CNTN5

4.54 PDE4D

2.83

2.49

2.79

3.55 RAPGEF2

2.59

Logical memory

2.22

2.17

2.49

4.22 RAB3C

1.92

2.48

2.24

3.34 LINC02233

3.84 SCNN1B

g Factor

1.90

2.25

3.33 CNTN5

3.31 MAST4

2.31

3.02

1.83

3.58 RAPGEF2

2.81

GHQ total

2.34

4.03 5’ RAB38

3.76 CNTN5

3.73 RNF180

2.15

3.12

1.80

2.84

3.26

MDD

2.22

3.04

2.03

3.74 PDE4D

2.83

2.35

2.79

3.27

3.93 HS3ST4

MDQ total

2.88

1.26

3.16

3.29

2.52

3.80 3KCNS3

2.63

2.62

2.93

SPQ total

2.42

3.13

2.17

3.91 MAST4

3.04

1.39

2.74

2.91

2.87

Age of onset

3.25

2.44

3.32 CNTN5

3.28

2.27

2.05

2.64

2.33

2.68

Episode count

2.84

2.17

3.55 CNTN5

2.53

3.24

1.99

2.52

1.90

3.54 HS3ST4

Region (Mb)

223–225

87.5–89

98.5–100.5

58–67

69–71

17.5–18.5

168–172

158–162

21–27

Genotyped SNPs

382

363

585

1511

297

214

698

563

1239

  1. Most significant p-value from case–control association analyses of imputed GWAS data in GS and UKB for affective disorder and for MDD and depression-related traits in GS (Supplementary Methods). Bold—p < 0.0005, -Log10 = 3.3