Table 2.

Genome-wide significant associations.

CHR	SNP	POSITION	Tested Allele	European ancestry		African ancestry
				OR	p-value	OR	p-value
19	rs8099917	39743165	G	0.385	5.24E-16	0.555	0.2309
6	rs6457620	32663999	G	0.605	1.47E-09	0.758	0.1571
6	rs6457617	32663851	C	0.614	3.43E-09	0.758	0.1573
6	rs9275224	32659878	A	0.615	4.76E-09	0.685	0.0550
6	rs6932517	32678182	C	0.600	1.10E-08	0.557	0.0064
6	rs9357152	32664960	G	1.664	1.20E-08	1.484	0.1075
6	rs9378125	32679732	G	1.657	1.57E-08	1.437	0.1397
6	rs2858324	32660375	A	0.604	2.89E-08	0.590	0.0178

List of variants that have genome-wide significant association with HCV spontaneous clearance (before imputation). The genomic position is in HG18.