TABLE 2.
Chr | SNP | hg38 | A1 | A2 | N | MAF | B | SE | p‐Value |
---|---|---|---|---|---|---|---|---|---|
13 | rs7330699 | 29,483,430 | G | A | 3,200 | 0.010 | 2.89 | 0.51 | 1.4 × 10−8 |
13 | rs73154407 | 29,483,753 | G | T | 3,184 | 0.010 | 2.97 | 0.51 | 7.6 × 10−9 |
13 | rs11842476 | 29,483,758 | G | A | 3,184 | 0.013 | 2.47 | 0.46 | 6.1 × 10−8 |
13 | rs73154410 | 29,483,772 | A | T | 3,187 | 0.010 | 2.96 | 0.51 | 7.8 × 10−9 |
13 | rs1350113738 | 29,483,860 | T | C | 3,184 | 0.010 | 2.88 | 0.51 | 1.5 × 10−8 |
13 | rs17073514 | 29,484,261 | G | T | 3,202 | 0.013 | 2.41 | 0.45 | 9.8 × 10−8 |
13 | rs116813765 | 29,484,326 | C | T | 3,204 | 0.010 | 2.89 | 0.51 | 1.4 × 10−8 |
13 | rs73154413 | 29,484,390 | C | T | 3,207 | 0.011 | 2.85 | 0.51 | 1.8 × 10−8 |
13 | rs73154414 | 29,484,568 | A | G | 3,201 | 0.010 | 2.91 | 0.51 | 1.2 × 10−8 |
13 | rs73154415 | 29,484,701 | A | G | 3,206 | 0.010 | 2.77 | 0.50 | 3.5 × 10−8 |
13 | rs41291229 | 29,484,987 | A | G | 3,186 | 0.010 | 2.75 | 0.50 | 4.0 × 10−8 |
Note: Physical positions in base pair (bp) correspond to the hg38 genome build.
Abbreviations: GWAS, genome‐wide association studies; MAF, minimum allele frequency; SNP, single nucleotide polymorphism.