Chr | Position (bp) | A1 | A2 | p-value | Genomic Region | Functional effect | Gene |
---|---|---|---|---|---|---|---|
Genome-wide significant SNPs | |||||||
 24 | 16,664,127 | G | T | 1.23E-07 | UTR3 | - | SMG1 |
 24 | 16,683,234 | G | A | 1.69E-07 | exon | synonymous | SMG1 |
 24 | 16,688,212 | T | C | 6.16E-07 | exon | synonymous | SMG1 |
Genome-wide suggestive SNPs | |||||||
 2 | 260,442,170 | C | T | 2.93E-06 | exon | synonymous | HSPG2 |
 9 | 100,456,022 | T | G | 4.49E-06 | intron | - | RALYL |
 8 | 13,714,405 | G | A | 9.38E-06 | UTR5 | - | CENPW |
 4 | 42,346,212 | T | G | 2.08E-05 | intron | - | PCLO |
 7 | 3,506,174 | C | G | 2.06E-05 | Intergenic | - | LOC106991156 (dist = 553,763); THBS1 (dist = 161,183) |
 15 | 57,714,827 | G | A | 3.66E-5 | intron | - | KLHL35 |