Table 4.
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) | Effect ± SE | -log10 (P) | MAF | (%) | Genese |
5 | 94.453 - 95.026 | rs136374794 | 94518850 | 11.633 | 120.3 ± 17.11 | 0.300 | 0.490 | rs136816685 | 95001236 | −80.76 ± 16.46 | 6.013 | 0.471 | 0.459 | PTPRO |
5 | 96.927 - 97.854 | rs110729080 | 97435197 | 8.791 | 149.8 ± 24.79 | 0.117 | 0.373 | rs134869818 | 97031962 | 97.04 ± 16.57 | 8.291 | 0.452 | 0.660 | GPRC5Af |
14 | 1.428 - 5.289 | rs109421300 | 1801116 | 134.354 | −389.4 ± 15.34 | 0.369 | 5.694 | rs109421300 | 1801116 | −234.1 ± 17.53 | 38.947 | 0.468 | 3.858 | DGAT1 f |
20 | 29.568 - 30.367 | rs134175348 | 30001269 | 7.230 | −104.6 ± 19.27 | 0.206 | 0.289 | rs42276093 | 29568029 | −133.9 ± 19.25 | 11.382 | 0.270 | 0.999 | NA |
aBTC: Bos Taurus chromosome
bIntervals containing individually validated SNPs are in bold
c MAF minor allele frequency
d σ 2a = additive 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