Table 2.
SNP | Chr | Position | Allele change | MAF | H-W(p-value) |
---|---|---|---|---|---|
rs78036292 | 7 | intron variant | T→ G | 0.0172 | 0.1635 |
rs6467431 | 7 | intron variant | G→ A | 0.3884 | 0.7747 |
rs67468325 | 7 | intron variant | A→ G | 0.0543 | 0.5127 |
rs1863015 | 7 | intron variant | A→ G | 0.4681 | 0.5225 |
rs156676 | 7 | intron variant | G→ A | 0.2644 | 0.0295 |
SNP, single nucleotide polymorphism; Chr, chromosome; MAF, minimum minor allele frequencies; H-W, Hardy-Weinberg equilibrium test.