TABLE 1.

Significant SNPs from linear regression and case-control GWAS. Table displaying information for significant SNPs identified in linear regression EMMAX GWAS with weaning tFEC phenotypes and recessive, dominant or additive inheritance models and case-control EMMAX GWAS with a recessive inheritance model. A, additive; CC, case-control; Chr, chromosome; D, dominant; FDR, false discovery rate; LR, linear regression; MAF, minor allele frequency; PVE, proportion of variance explained; R, recessive.

Model	Chr	rs Number	Position bp	P-Value		MAF	PVE	Gene
				Unadjusted	FDR
LR-R	5	rs405327900	88,129,857	3.34e-08	0.0169	0.3532	0.0539	EDIL3
	5	rs413712238	88,154,411	3.34e-08	0.0084	0.3511	0.0539
	5	rs417983470	88,160,689	6.66e-08	0.0112	0.3511	0.0516
	5	rs416102123	88,144,942	7.82e-08	0.0099	0.3500	0.0511
LR-A	2	rs428768700	14,076,309	1.49e-08	0.0075	0.0214	0.0567	PALM2AKAP2
LR-D	2	rs428768700	14,076,309	1.49e-08	0.0075	0.0214	0.0567	PALM2AKAP2
	10	rs417380632	6,660,635	2.32e-07	0.0588	0.3671	0.0475	24 kpb 5′ of PCDH17
CC-R	9	rs416881989	5,046,485	1.01e-08	0.0051	0.4218	0.0580	ADGRB3
	9	rs421657777	5,325,635	5.81e-08	0.0147	0.4786	0.0521