highly significant-log 10 ( P ) = 13.7
SYN25051 (A/G), the most highly significant SNP with -log 10 ( P ) = 13.7 at position 161,275,547 on Chr2, explained 27.1% of the phenotype variation.
SYN25051 (A/G), the most highly significant SNP with -log 10 ( P ) = 13.7 at position 161,275,547 on Chr2, explained 27.1% of the phenotype variation.