Table 3.
SSC | Interval | Top SNP of the GWAS interval | # SNPs called | Highest LD | SNP with highest LD | Genotypic frequency (0/0; 0/1; 1/1) | # called samples | SNP effect | Gene | Trait |
---|---|---|---|---|---|---|---|---|---|---|
1 | I3 | rs327733412 | 3 | 0.07 | rs710447566 | 0.34; 0.54; 0.11 | 35 | Low | KATNAL2 | HABN |
7 | I2 | rs336588919 | 2 | 0.4 | rs330912302 | 0.63; 0.12; 0.25 | 32 | Low | CHD2 | NABN |
13 | I1 | rs690794887 | 21 | 0.4 | rs331304027 | 0.06; 0.09; 0.85 | 33 | Moderate | ULK4 | HABN |
13 | I2 | rs327865244 | 11 | 0.2 | rs323872641 | 0.49; 0.37; 0.14 | 35 | Low | ABHD14A | HABN |
SSC, Sus scrofa chromosome; # SNPs called, number of SNPs identified in the SNP calling analysis; LD, linkage disequilibrium; Genotypic frequency: allelic frequency for each of the genotypes; # called samples, number of samples with reads in the given SNP position; HABN, head abnormalities; NABN, neck abnormalities
The columns SNP effect and gene refer to the SNP with the highest LD in the region