Table 1.
SNP I.D. | Trait of interest | Chr_mb | Zscore | P-value | Nearby gene | SNP location relative to gene |
---|---|---|---|---|---|---|
rs43555985 | RFI | 8_69 | −4.458 | 8.28E-06 | GFRA2 | 53.4 kb upstream |
rs41638273 | RFI | 2_6 | 4.4 | 1.08E-05 | SLC40A1 | 15.7 kb upstream |
rs109695205 | RFI | 5_113 | 4.313 | 1.61E-05 | NFAM1 | 26.5 kb upstream |
rs110161277 | RFI | 2_2 | 4.192 | 2.76E-05 | PLEKHB2 | 143.8 kb downstream |
rs110418027 | RFI | 5_116 | −4.089 | 4.34E-05 | SMC1B | Intron variant |
rs43691372 | RFI | 12_47 | 4.082 | 4.47E-05 | DIS3 | 3′ UTR variant |
rs42820242 | RFI | 14_44 | 4.081 | 4.48E-05 | IL7 | 104.2 kb downstream |
rs386023985 | ADG | 19_48 | −6.593 | 4.32E-11 | ERN1 | 7.9 kb upstream |
rs135897656 | ADG | 3_119 | 6.195 | 5.83E-10 | CSF2RA | Intron variant |
rs136457441 | ADG | 19_28 | 5.936 | 2.93E-09 | RPL26 | Missense variant |
rs110660154 | ADG | 1_19 | 5.314 | 1.08E-07 | SPATA16 | 265 kb downstream |
rs110780286 | ADG | 18_15 | 4.492 | 7.06E-06 | ITFG1 | Intron variant |
rs382426807 | ADG | 19_43 | 4.473 | 7.70E-06 | STAT5A | Synonymous variant |
rs41595251 | ADG | 9_91 | −4.375 | 1.22E-05 | OPRM1 | 269 kb upstream |
rs110590483 | ADG | 11_39 | −4.243 | 2.21E-05 | CCDC85A | 509 kb downstream |
rs109252082 | ADG | 19_53 | 4.124 | 3.72E-05 | TBC1D16 | Intron variant |
rs41592667 | ADG | 9_35 | 4.12 | 3.78E-05 | FRK | 88 kb downstream |
rs41630180 | ADG | 17_1 | −4.097 | 4.18E-05 | TLL1 | Intron variant |
rs41614223 | ADG | 9_27 | −4.086 | 4.39E-05 | NKAIN2 | 8.8 kb downstream |
rs137576435 | ADG | 19_12 | −4.079 | 4.52E-05 | BCAS3 | Intron variant |
rs136789347 | ADG | 23_52 | −4.069 | 4.72E-05 | OR5M10 | 13.8 kb upstream |
IDBV32000008978 | FI | 20_67 | 4.355 | 1.33E-05 | ADAMTS16 | Synonymous variant |
rs55617218 | FI | 19_14 | −4.205 | 2.61E-05 | HNF1B | Intron variant |
rs109691080 | FI | 1_6 | 4.084 | 4.43E-05 | MAP3K7CL | 58.9 kb upstream |
SNP: Single nucleotide polymorphism; RFI: Residual feed intake; ADG: Average daily gain; FI: Feed intake; Chr_mb: Chromosome_megabase.