Table 2.

Significant loci associated with inguinal hernia among patients at BioBank Japan Project identified by genome-wide association study

Chr	Position	SNP id (rs)	Gene	Ref/var	Location	AF.Cases	AF.Controls	OR	95% CI	p-value
7	73389541	rs118109209	ELN/TMEM270	A/T	Intergenic	0.071	0.052	1.64	1.25, 2.15	4.7 × 10−9

Allele frequencies in the 1000 Genomes: East Asian A=0.9742, T=0.0258; Europe A=1.0000, T=0.0000.

Chr, chromosome; Ref, reference allele; Var, variant allele; AF.Cases, variant allele frequency in cases; AF.Controls, variant allele frequency in controls; OR, odds ratio; CI, confidence interval.