TABLE 2.

Heritability estimated from variants associated with GC risk.

Modela	h2(SE) observed scale	h2(SE) liability scale
		Prevalence	Prevalence	Prevalence
		(32.43/100,000)	(42.43/100,000)	(52.43/100,000)
SNPs identified by previous GWAS (n = 19)a	3.50%	1.14%	1.19%	1.23%
The identified eSNPs (n = 4)b	1.80%	0.58%	0.60%	0.62%
The identified eSNPs in unknown loci (n = 2)c	0.49%	0.16%	0.16%	0.17%
Combination (n = 21)d	3.96%	1.30%	1.35%	1.39%

^aVariants reported by previous GWAS studies. ^bSignificant eSNPs identified by the present study. ^cSignificant novel eSNPs identified by the present study. ^dConsist of 19 GWAS reported SNPs and 2 novel identified eSNPs by present study.