rsID
|
Chr
|
Position
|
A1a
|
OR
|
95% CI
|
P value
|
Nearest genes
|
---|
rs61828386
|
1
|
172863647
|
G
|
0.69
|
0.58–0.82
|
1.79 × 10−5
|
TNFSF18, FASLG
|
rs67164098
|
2
|
68556131
|
A
|
1.67
|
1.31–2.13
|
4.65 × 10−5
|
CNRIP1
|
rs11681966
|
2
|
100759457
|
C
|
1.50
|
1.23–1.78
|
4.04 × 10−5
|
AFF3
b
|
rs10758368
|
9
|
36310778
|
A
|
0.70
|
0.58–0.83
|
5.48 × 10−5
|
RNF38
|
rs9533119
|
13
|
43049426
|
A
|
1.36
|
1.17–1.59
|
6.32 × 10−5
|
TNFSF11
|
rs2934178
|
15
|
48218221
|
C
|
0.70
|
0.59–0.82
|
2.96 × 10−5
|
SEMA6D
|
- Chr: chromosome.
- aThe test allele and minor allele for this the study.
- bIndicates a validated risk locus for RA.