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. 2021 Jul 27;24(1):47–56. doi: 10.2478/bjmg-2021-0004

Table 2.

Single nucleotide polymorphism information and Hardy-Weinberg p values in the study population.

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