Table 4. Highly significant SNPs identified in AUCinf group following regression analysis (P<0.0001).
| Name | chr | Gene | Location | g1 | n1 | m1 | s1 | g2 | n2 | m2 | s2 | P VALUE |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11165069 | 1 | ABCA4 | intron | CC | 22 | 908.30 | 573.63 | TC | 1 | 4073.42 | 0.00002 | |
| rs1051640 | 17 | ABCC3 | synonymous | AA | 22 | 908.30 | 573.63 | AG | 1 | 4073.42 | 0.00002 | |
| rs2291550 | 12 | ABCC9 | synonymous | CC | 22 | 908.30 | 573.63 | TC | 1 | 4073.42 | 0.00002 | |
| rs17847036 | 10 | CYP2C9 | synonymous | AG | 1 | 4073.42 | GG | 22 | 908.30 | 573.63 | 0.00002 | |
| rs12461006 | 19 | SLC1A6 | intron | AG | 2 | 3049.93 | 1447.43 | GG | 21 | 855.06 | 529.17 | 0.00008 |
| rs4646196 | 5 | SLC22A4 | intron | AG | 1 | 4073.42 | GG | 22 | 908.30 | 573.63 | 0.00002 | |
| rs757220 | 19 | SLC25A42 | intron | CC | 22 | 908.30 | 573.63 | TC | 1 | 4073.42 | 0.00002 | |
| rs7248399 | 19 | SLC25A42 | intron | AG | 1 | 4073.42 | GG | 22 | 908.30 | 573.63 | 0.00002 | |
| rs10417974 | 19 | SLC25A42 | 3UTR | TC | 1 | 4073.42 | TT | 22 | 908.30 | 573.63 | 0.00002 | |
| rs4980343 | 15 | SLC28A1 | intron | AG | 1 | 4073.42 | GG | 22 | 908.30 | 573.63 | 0.00002 | |
| rs12150890 | 19 | SLC7A9 | synonymous | AA | 22 | 908.30 | 573.63 | AG | 1 | 4073.42 | 0.00002 | |
| rs7637682 | 3 | SLC9A10 | intron | AA | 22 | 908.30 | 573.63 | AG | 1 | 4073.42 | 0.00002 | |
| rs4234409 | 3 | SLC9A10 | intron | AA | 22 | 908.30 | 573.63 | AC | 1 | 4073.42 | 0.00002 | |
| rs4434123 | 3 | SLC9A10 | missense | AA | 22 | 908.30 | 573.63 | AG | 1 | 4073.42 | 0.00002 | |
| rs17446282 | 3 | SLC9A10 | intron | AA | 22 | 908.30 | 573.63 | AG | 1 | 4073.42 | 0.00002 | |
| rs6781844 | 3 | SLC9A10 | missense | TG | 1 | 4073.42 | TT | 22 | 908.30 | 573.63 | 0.00002 | |
| rs9855755 | 3 | SLC9A10 | intron | AG | 1 | 4073.42 | GG | 22 | 908.30 | 573.63 | 0.00002 | |
| rs17724104 | 20 | SLC9A8 | intron | AA | 22 | 908.30 | 573.63 | AG | 1 | 4073.42 | 0.00002 |
Abbreviations: Chr, chromosome; N, number, g1, genotype 1, n1, number 1; s1, standard deviation 1; g2, genotype 2; n2, number 2; s2, standard deviation 2 *Table only shows several SNPs from a total of 1498 highly significant SNPs.