Table 1 Variants detected by whole genome resequencing of two cases, two obligate carriers, and 75 controls
Filtering StepNumber of Variants
Variants with genotypes 1/1 in cases and 0/1 in carriers53,683
NFS-associated variants in whole genomea351
NFS-associated variants in critical interval on chr. 27a0
NFS-associated variants in critical interval on chr. 7a4
NFS-associated nonsynonymous variants in critical intervalsa1
  • a “NFS-associated” indicates variants that were homozygous for the alternate allele in the two cases, heterozygous in the two carriers, and homozygous reference (or missing) in the 75 control horses.