Table 1 Conventional GWAS GenLang selected subset only.

From: Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

SNP

Position

A1

Freq

Gene

Effect

SE

P

N

rs4818369

21:19055075

T

0.60

BTG3-C21orf91

−0.15

2.43 × 10–2

2.37 × 10–10

4152

  1. SNP Single Nucleotide Polymorphism, Position chromosome: base pair (hg19), A1 Allele 1, Freq Allele Frequency, SE Standard Error, P P value, N Sample Size.
  2. Only genome-wide significant results shown (significance threshold p = 5 × 10−8).
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