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Table 3 Index SNPs from independent chromosomal regions showing borderline significant association with repeated measures of response at 3 and 6 months

From: A longitudinal genome-wide association study of anti-tumor necrosis factor response among Japanese patients with rheumatoid arthritis

SNP

Chr

Position (bp)

Minor allele

MAF

Genotype

N

β (95 % CI)

P value

Gene(s) in region of association

rs284515

6

91,208,828

G

0.17

AG/GG

134

0.35 (0.21, 0.49)

6.6×10−7

MAP3K7, BACH2

     

AG

121

0.33 (0.16, 0.51)

2.1×10−4

     

GG

13

0.80 (0.43, 1.18)

2.6×10−5

rs75908454

6

169,970,623

C

0.10

CT/CC

88

0.42 (0.26, 0.59)

6.3×10−7

WDR27

     

CT

87

0.41 (0.24, 0.59)

2.3×10−6

     

CC

1

-

-

rs1679568

10

117,817,551

A

0.15

AG/AA

124

0.35 (0.21, 0.49)

8.1×10−7

GFRA1

     

AG

114

0.37 (0.20, 0.54)

1.6×10−5

     

AA

10

0.63 (0.24, 1.02)

1.6×10−3

  1. The single nucleotide polymorphisms (SNP) with the smallest p value (index SNP) in each of the associated regions are shown. β (regression coefficient) represents the increase in change in DAS28 associated with the genotype(s) shown compared to the reference genotype (with no minor alleles). Chr chromosome, MAF minor allele frequency, N number of patients with genotype(s) shown