Skip to main content

View full-text article in PMC

. 2017 Feb 22;7(4):1315–1321. doi: 10.1534/g3.117.039511

Table 1. Variants detected by whole genome resequencing of two cases, two obligate carriers, and 75 controls.

Filtering Step	Number of Variants
Variants with genotypes 1/1 in cases and 0/1 in carriers	53,683
NFS-associated variants in whole genome^a	351
NFS-associated variants in critical interval on chr. 27^a	0
NFS-associated variants in critical interval on chr. 7^a	4
NFS-associated nonsynonymous variants in critical intervals^a	1

^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.