Table 2.
SNP | Gene/ Closest Gene | Chromosomal Position | Location | Allele Change | Amino Acid Change | HWE p Value |
---|---|---|---|---|---|---|
rs10783050 | EEF1A1P11-RPL7P9 | 1:96571527 | intergenic | T>C | – | 0.932 |
rs1143623 | IL1B | 2:112838252 | intergenic | C>G | – | 0.309 |
rs13266634 | SLC30A8 | 8:117172544 | missense | C>A/T | Arg325Trp | 0.532 |
rs13376631 | FMO1 | 1:171266603 | intron | A>G | – | 0.903 |
rs1801282 | PPARG | 3:12351626 | missense | C>G | Pro12Ala | monomorphic |
rs249429 | PRKAA1 | 5:40782137 | intron | C>T | – | 0.299 |
rs2815752 | NEGR1 | 1:72346757 | intergenic | G>A | – | 0.636 |
rs316009 | SLC22A2 | 6:160254732 | intron | C>T/G | – | 0.595 |
rs316019 | SLC22A2 | 6:160249250 | missense | C>A | Ala270Ser | 0.808 |
rs391300 | SRR | 17:2312964 | intron | C>T | – | 0.739 |
rs461473 | SLC22A1 | 6:160122530 | intron | G>A | – | 0.898 |
rs4810083 | PCK1 | 20:57545215 | intergenic | C>T | – | 0.145 |
rs578427 | – | 6:91702432 | intergenic | T>C | – | 0.909 |
rs622342 | SLC22A1 | 6:160151834 | intron | A>C | – | 0.218 |
rs6265 | BDNF; BDNF-AS | 11:27658369 | missense | C>T | Val66Met | monomorphic |
rs819 2675 | SLC2A2 | 3:171007094 | intron | C>T | – | 0.674 |