Table 1.

Illustration of the first rows in the table generated by GWEHS (Genome-Wide Effect size and Heritability Screener), showing example data for Digestive disease (i.e., Crohn’s disease and Inflammatory bowel disease), using the default parameters.

Trait	PMID	locus	SNP	effect	q	h2	−logP
Crohn’s disease	23128233	AC007728.2	rs2066847	0.383	0.024	0.007	208.222
Crohn’s disease	30500874	HLA-DQB1–MTCO3P1	rs184950714	0.209	0.156	0.011	18.398
Crohn’s disease	18587394	LINC02471	rs11175593	0.143	0.020	0.001	9.523
Crohn’s disease	22412388	LINC00491	rs7705924	0.124	0.066	0.002	7.699
Crohn’s disease	26192919	SLC2A13–LINC02555	rs12422544	0.124	0.019	0.001	24.398
Crohn’s disease	17554261	LINC01680–AL359081.1	rs10801047	0.120	0.080	0.002	7.523
Crohn’s disease	23850713	FCHSD2–AP002761.2	rs11235667	0.117	0.096	0.002	8.155
Crohn’s disease	22412388	AL645939.5	rs9258260	0.114	0.104	0.002	9.699
Crohn’s disease	21102463	NOD2	rs2076756	0.112	0.260	0.005	68.398

The table shows the SNPs sorted by decreasing effect size, including information on the trait name (Trait), publication (PMID), mapped gene or inter-genic region (locus), SNP identifier (SNP), effect size (effect), risk allele frequency (q), contribution to heritability (h²) and probability value (−logP).