Table 2 Genome-wide significant associations.

From: Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection

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

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