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. 2020 Nov 19;11(11):1369. doi: 10.3390/genes11111369

Table 1.

Candidate SNPs identified from the exploratory GWAS. A1 indicates the minor allele (i.e., least frequently observed based on the whole sample); F_A and F_U indicate the frequency of the minor allele in the affected and unaffected cats, respectively. The p value is shown calculated by Fisher’s Exact test and Bonferroni corrected by PLINK. No odds ratio could be calculated for SNP2 because the associated allele was not found in unaffected cats. SNPs were named in the Illumina array only as custom numbers; for convenience, they are named here as SNPs 1 to 6.

SNP Illumina No. A1 F_A F_U p Odds Ratio
SNP1 10566 G 0.75 0.15 0.00014 17
SNP2 10762 G 0.5 0 0.00026 NA
SNP3 30747 G 0.1 0.65 0.00033 0.059
SNP4 36147 G 0.8 0.2 0.00015 16
SNP5 36165 A 0.1 0.65 0.00033 0.059
SNP6 36166 A 0.1 0.65 0.00033 0.059