Table 4.
Hypothesis | SNP | Position | Gene | P GWAS | qSFDR |
---|---|---|---|---|---|
Neuronal Migration/Axon Guidance | rs4818369 | 21:19055075 | BTG3-C21orf91** | 2.37 × 10–10 | 9.00 × 10–4 |
rs6090818 | 20.:46883131 | LINC00494** | 1.82 × 10–7 | 3.67 × 10–2 | |
rs6865160 | 5:31766737 | PDZD2 | 2.82 × 10–7 | 4.10 × 10–2 | |
SFARI ASD | rs4818369 | 21:19055075 | BTG3-C21orf91** | 2.37 × 10–10 | 8.00 × 10–4 |
rs6090818 | 20.:46883131 | LINC00494** | 1.82 × 10–7 | 3.50 × 10–2 | |
rs6865160 | 5:31766737 | PDZD2 | 2.82 × 10–7 | 3.92 × 10–2 |
Total SNPs: ~5,610,600.
Upweighted SNPs: Neuronal migration, 116,829; SFARI ASD 371,158.
SNP Single Nucleotide Polymorphism, Position chromosome: base pair (hg19), P GWAS P-value in GWAS, qSFDR q-value from SFDR program.
Additional information including LD SNPs or SNPs in same gene region, rank and up-weighted status in the supplementary material.
Significance threshold q ≤ 2.5 × 10−2.
**Intergenic and associated with word reading in Gialluisi et al., (6.79 × 10−6/3.14 × 10−7).