Table 6.
Most strongly associated SNP in discovery | Most strongly associated SNP in validation | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
BTCa | Interval (Mbp)b | SNP | Position (bp) | -log10 (P) | Effect ± SE | MAFc | (%)d | SNP | Position (bp) | -log10 (P) | Effect ± SE | MAF | (%) | Genese |
2 | 95.312 - 95.730 | rs136022579 | 95312328 | 4.920 | 155 ± 35.39 | 0.166 | 0.149 | rs134324850 | 95725812 | 3.563 | 132 ± 36.23 | 0.171 | 0.197 | ADAM23 |
3 | 97.907 - 98.799 | rs43361287 | 98306933 | 4.351 | 82.29 ± 20.14 | 0.443 | 0.133 | rs43363311 | 97907057 | 2.516 | 64.04 ± 21.6 | 0.427 | 0.139 | AGBL4 |
5 | 71.878 - 71.878 | rs110106971 | 71878168 | 4.947 | −99.82 ± 22.71 | 0.332 | 0.158 | rs110106971 | 71878168 | 2.012 | 55.58 ± 21.49 | 0.438 | 0.106 | SYN3 f |
26 | 32.249 - 32.341 | rs42460360 | 32248251 | 4.185 | 129.5 ± 32.42 | 0.186 | 0.124 | rs42741343 | 32336734 | 2.065 | 61.42 ± 23.36 | 0.349 | 0.110 | LOC100847832 |
26 | 39.358 - 39.765 | rs132810457 | 39358269 | 4.017 | 86.38 ± 22.13 | 0.343 | 0.122 | rs110552548 | 39764774 | 2.239 | −88.38 ± 32 | 0.214 | 0.125 | GRK5 |
26 | 44.215 - 44.543 | rs109406756 | 44537471 | 4.673 | 114.1 ± 26.83 | 0.244 | 0.143 | rs134524557 | 44257893 | 2.246 | 70.3 ± 25.4 | 0.301 | 0.123 | LHPP |
27 | 42.674 - 42.890 | rs41665573 | 42837186 | 5.248 | −90.48 ± 19.92 | 0.469 | 0.164 | rs41575082 | 42673983 | 2.328 | 62.09 ± 21.95 | 0.424 | 0.130 | NA |
aBTC: Bos Taurus chromosome
bIntervals containing individually validated SNPs are in bold
cMAF: minor allele frequency
d σ 2d = dominance variance; σ 2p = phenotypic variance
eGenes with both top SNPs in discovery and validation inside them are in bold
fGenes with individually validated SNPs within them