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. 2019 Jun 19;56(9):607–616. doi: 10.1136/jmedgenet-2018-105965

Table 2.

Significant loci associating with the circulating inflammatory phenotypes

Study Marker Locus Chr:Position Candidate gene Nearest gene(s) Annotation dbSNP reference INFO EA EAF Beta P value HetPVal Variance explained Total variance explained
NFBC1966 sE-selectin 9q34.2 9:136 141 870 ABO ABO Intronic rs2519093 0.994 T 0.188 −0.903 4.48e-305 NA 0.249 0.258
11q24.2 11:126 266 665 ST3GAL4 ST3GAL4 Intronic rs11220471 0.967 G 0.212 0.162 7.72e-12 NA 0.009
sICAM-1 9q34.2 9:136 141 870 ABO ABO Intronic rs2519093 0.994 T 0.188 −0.352 7.43e-48 NA 0.038 0.118
19p13.2 19:10 383 403 ICAM1 ICAM1 Intronic rs117960796 0.802 A 0.012 −1.669 8.03e-40 NA 0.066
19p13.2 19:10 497 360 ICAM1 CDC37 Intergenic rs74428614 0.992 A 0.163 0.226 1.14e-16* NA 0.014
sVCAM-1 9q34.2 9:136 131 322 ABO ABO Missense rs8176746 1.000 T 0.129 0.256 5.06e-19 NA 0.015 0.038
12q23.3 12:104 448 391 HSP90B1 GLT8D2 Intronic rs117238625 0.981 A 0.023 0.510 2.90e-14 NA 0.012
17q24.2 17:66 823 805 ABCA8 ABCA8 Intergenic rs112001035 0.883 A 0.060 0.324 1.04e-13 NA 0.012
Meta-analyses IL1β 6p22.1 6:30 017 071 HLA locus Intronic rs6917603 1.000 C 0.251 0.163 1.76e-12 1.00 0.010 0.015
6p22.1 6:30 013 887 HLA locus Intronic rs9261224 1.000 T 0.035 0.261 1.31e-09 * 1.00 0.005
IP10 4q21.1 4:76 899 176 CXCL10 SAD1 Intronic rs192716315 0.851 C 0.003 1.513 2.71e-13 1.00 0.014 0.014
MCP1 1q23.2 1:159 175 354 ACKR1 ACKR1 Missense rs12075 1.000 A 0.469 0.148 1.43e-33 1.51e-13 0.011 0.011
TNFα 13q14.3 13:51 141 997 DLEU1 DLEU1 Intronic rs17074575 0.803 G 0.002 2.131 2.71e-09 1.00 0.018 0.018
VEGF 4p16.2 4:5 636 073 STK32B EVC2 Intronic rs186725382 0.875 A 0.001 2.380 4.53e-10 1.00 0.011 0.052
6p21.1 6:43 927 050 VEGFA C6orf223 Intergenic rs7767396 1.000 A 0.523 0.284 8.35e-105 1.22e-69 0.040 0.056
9p24.2 9:2 686 273 VLDLR VLDLR, KCNV2 Intergenic rs7030781 0.959 T 0.373 -0.099 1.57e-13 5.34e-04 0.005

Statistical significance is considered at p<3.1×10−9. Novel findings are highlighted with bold font. All positions correspond to human genome build 37.

*Indicates associations that are significant after conditioning the analyses on the locus-specific lead variant on the preceding row.

EA, effect allele; EAF, effect allele frequency; HLA, human leukocyte antigen; HetPVal, p value of heterogeneity as estimated by Cochrane’s Q-test; IL1β, interleukin 1-beta; INFO, imputation score in NFBC1966; IP10, interferon gamma-induced protein 10; MCP1, monocyte chemoattractant protein 1; NA, not available; NA, not available; NFBC1966, Northern Finland Birth Cohort 1966; TNFα, tumour necrosis factor alpha; VEGF, vascular endothelial growth factor; dbSNP, single nucleotide polymorphism database; sE-selectin, soluble E-selectin; sICAM-1, soluble intercellular adhesion molecule -1; sVCAM-1, soluble vascular cell adhesion molecule-1.