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Table 3 Association results for the lead signals from the discovery analysis

From: Common variation contributes to the genetic architecture of social communication traits

 

Nearest

Discovery (N = 5,584)

Replication (N = 1,364)

Combined (N = 6,948)

SNP

Chr

E,A

Gene

EAF

β (SE)a

P a

EAF

β (SE)

P

β (SE)

P

Het-P

rs761490

1p32.3

C,G

TMEM48

0.24

0.096 (0.022)

9.7E-06

0.23

−0.051 (0.090)

0.57

0.088 (0.021)

3.0E-05

0.11

rs9257616

6p22.1

G,A

OR2J2

0.56

0.086 (0.018)

3.1E-06

0.54

0.19 (0.074)

0.009

0.093 (0.018)

2.5E-07

0.16

rs12115663

9p22.3

C,A

BNC2

0.86

0.13 (0.027)

4.1E-06

0.87

−0.12 (0.10)

0.23

0.11 (0.026)

3.6E-05

0.018

rs1834180

10q25.1

A,G

intergenic

0.68

0.10 (0.020)

3.3E-07

0.70

0.033 (0.079)

0.68

0.097 (0.019)

4.6E-07

0.40

rs2352908

14q22.1

G,T

intergenic

0.84

0.11 (0.026)

8.2E-06

0.83

0.24 (0.10)

0.022

0.12 (0.025)

1.1E-06

0.25

rs11625667

14q24.3

G,A

TMEM90A

0.36

0.085 (0.018)

4.3E-06

0.35

−0.049 (0.076)

0.52

0.077 (0.018)

1.7E-05

0.086

rs4218

15q22.2

G,C

MYO1E

0.29

0.11 (0.020)

2.6E-08

0.31

−0.027 (0.080)

0.74

0.10 (0.019)

1.0E-07

0.096

  1. a - Genomic-control corrected.
  2. Results are presented for the most significant signals (Genomic-control corrected P ≤1E-05) from independent loci during the discovery stage of the analysis. Regression estimates were obtained using Quasi-Poisson regression. All SNPs were imputed and had an imputation quality of 0.90 <R2 ≤0.99 (MACH); Replicated signals are indicated in bold. E, Effect allele; A, Alternative allele; EAF, Effect allele frequency; Het-P, Heterogeneity P- value.