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. 2016 May 1;193(9):1008–1022. doi: 10.1164/rccm.201507-1372OC

Table 2.

Results of Immunochip Analysis on Non-LS versus Healthy Control Subjects Highlighting the Top 25 SNPs at Significance P Less Than 5 × 10−8

SNP CHR BP Gene (Nearby Genes) CA/NCA CAF Discovery Cohort (Sweden, European Ancestry) (n = 2,750)
Replicating Cohort (Germany, European Ancestry) (n = 4,911)
Replicating Cohort (African American Ancestry) (n = 1,657)
OR (95% CI) P Value PGC OR (95% CI) P Value OR (95% CI) P Value
rs1964995 6 32557389 (HLA-DRA, HLA-DRB5) G/A 0.296 0.55 (0.47–0.64) 2.47E-15 2.57E-13 0.56 (0.48–0.66) 1.19E-12 0.70 (0.59–0.82) 1.95E-05
rs9269110 6 32551247 (HLA-DRA, HLA-DRB5) A/C 0.389 1.74 (1.51–2.01) 5.78E-14 3.82E-12 1.34 (1.16–1.56) 6.20E-05
rs9269081 6 32549078 (HLA-DRA, HLA-DRB5) A/C 0.376 1.71 (1.48–1.97) 4.01E-13 2.01E-11 1.33 (1.14–1.54) 1.63E-04
rs6923504 6 32536164 (HLA-DRA, HLA-DRB5) G/C 0.381 1.66 (1.44–1.91) 4.05E-12 1.46E-10 1.35 (1.16–1.56) 6.09E-05
rs6903608 6 32536263 (HLA-DRA, HLA-DRB5) G/A 0.381 1.66 (1.44–1.91) 4.05E-12 1.46E-10 1.36 (1.17–1.57) 3.55E-05
rs9268882 6 32539601 (HLA-DRA, HLA-DRB5) A/G 0.381 1.66 (1.44–1.91) 4.54E-12 1.61E-10 1.36 (1.17–1.57) 3.86E-05
rs3998158 6 32789970 (HLA-DQB1, HLA-DQA2) G/A 0.168 0.53 (0.45–0.64) 5.35E-12 1.85E-10 0.60 (0.49–0.74) 9.45E-07 1.19 (0.98–1.43) 7.47E-02
rs9275582 6 32788048 (HLA-DQB1, HLA-DQA2) A/G 0.172 0.53 (0.45–0.64) 5.56E-12 1.91E-10 0.59 (0.48–0.72) 2.42E-07 1.29 (1.08–1.54) 4.29E-03
rs9275580 6 32787440 (HLA-DQB1, HLA-DQA2) G/A 0.178 0.54 (0.46–0.65) 9.71E-12 3.08E-10 0.60 (0.50–0.74) 4.99E-07 1.42 (1.20–1.67) 3.98E-05
rs2395153 6 32453573 (C6orf10, BTNL2) C/G 0.273 0.59 (0.51–0.69) 1.46E-11 4.38E-10 0.68 (0.58–0.79) 8.61E-07 0.63 (0.53–0.75) 2.12E-07
rs3129948 6 32462622 (C6orf10, BTNL2) C/A 0.390 1.63 (1.41–1.88) 4.11E-11 1.06E-09 1.35 (1.17–1.56 5.66E-05 1.35 (1.14–1.60) 6.34E-04
rs3117098 6 32466491 (C6orf10, BTNL2) G/A 0.390 1.59 (1.38–1.84) 2.37E-10 4.78E-09 1.35 (1.16–1.56) 6.45E-05 1.36 (1.14–1.61) 4.63E-04
rs3129954 6 32473558 BTNL2 A/G 0.390 1.59 (1.38–1.84) 2.37E-10 4.78E-09 1.35 (1.16–1.56) 6.10E-05 1.34 (1.13–1.59) 8.91E-04
rs4424066 6 32462406 (C6orf10, BTNL2) G/A 0.314 0.62 (0.54–0.72) 2.54E-10 5.06E-09 0.70 (0.60–0.81) 3.09E-06 0.75 (0.64–0.87) 1.97E-04
rs3129961 6 32486918 (BTNL2, HLA-DRA) G/A 0.390 1.59 (1.38–1.84) 2.82E-10 5.53E-09 1.34 (1.16–1.55) 7.52E-05 1.35 (1.14–1.60) 4.18E-04
rs3129955 6 32473818 BTNL2 A/G 0.385 1.59 (1.38–1.84) 3.49E-10 6.64E-09 1.35 (1.17–1.56) 5.19E-05 1.34 (1.13–1.59) 8.24E-04
rs4373382 6 32458846 (C6orf10, BTNL2) C/A 0.313 0.63 (0.54–0.73) 4.16E-10 7.72E-09 0.69 (0.59–0.80) 1.58E-06 0.75 (0.65–0.87) 1.73E-04
rs3817973 6 32469089 (C6orf10, BTNL2) A/G 0.314 0.63 (0.54–0.73) 4.35E-10 8.02E-09 0.69 (0.59–0.80) 1.57E-06 0.75 (0.65–0.88) 2.68E-04
rs2076529 6 32471933 BTNL2 G/A 0.314 0.63 (0.54–0.73) 4.35E-10 8.02E-09 0.69 (0.59–0.80) 1.48E-06 0.75 (0.65–0.88) 2.56E-04
rs9268472 6 32463583 (C6orf10, BTNL2) A/G 0.314 0.63 (0.54–0.73) 4.61E-10 8.43E-09 0.69 (0.59–0.80) 1.57E-06 0.76 (0.65–0.89) 4.44E-04
rs9271588 6 32698931 (HLA-DRB1, HLA-DQA1) G/A 0.351 0.64 (0.56–0.74) 8.35E-10 1.40E-08 0.67 (0.58–0.78) 2.40E-07
rs2858332 6 32789139 (HLA-DQB1, HLA-DQA2) A/C 0.354 0.65 (0.56–0.75) 1.47E-09 2.28E-08 1.36 (1.18–1.57) 3.07E-05
rs3830135 6 32656442 HLA-DRB1 A/G 0.054 0.42 (0.32–0.56) 1.82E-09 2.74E-08 0.56 (0.42–0.74) 3.16E-05

Definition of abbreviations: BP = base pairs; CA = coded allele; CAF = coded allele frequency; CHR = chromosome; CI = confidence interval; LS = Löfgren’s syndrome; NCA = noncoded allele; OR = odds ratio; P = unadjusted P value; PGC = adjusted P value by genomic control (lambda = 1.17); SNP = single-nucleotide polymorphism.

Genetic effects (OR) adjusted according to sex, coded allele. OR is the risk on LS (0/1) per allele based on the additive genetic model. 95% CI is the 95% CI for the OR.

The entire list of non-LS–associated SNPs is provided in Table E3.