Table 2.
SNPb | Exp(Beta)c | 95% CI | P | Location | MAF | Gene |
---|---|---|---|---|---|---|
rs17200810d | 1.65 | (1.35, 2.02) | 1.41×10−6 | 3’ | 0.02 | TNF |
rs34451538 | 1.50 | (1.26, 1.79) | 3.90×10−6 | 5’ | 0.03 | TNF |
rs276565e | 1.11 | (1.06, 1.16) | 5.30×10−6 | 5’ | 0.28 | IFNGR1f |
rs114064880 | 1.71 | (1.36, 2.16) | 5.33×10−6 | 5’ | 0.01 | TNF |
rs11575838 | 1.68 | (1.34, 2.11) | 7.13×10−6 | 3’ | 0.01 | TNF |
rs2770148g | 1.15 | (1.08, 1.23) | 2.94×10−5 | Intron 2 | 0.12 | TLR4 |
Abbreviations: KT, kynurenine/tryptophan ratio; SNP, single nucleotide polymorphism; CI, confidence interval; MAF, minor allele frequency.
Linear mixed effects regression models of log10plasma KT ratio were adjusted for gender, pregnancy, cohort (ARKS vs. UARTO), and the first ten principal components.
Genotyped or imputed single nucleotide polymorphism.
Fold change in KT ratio (nM/μM) per copy of minor allele.
Genotyped SNP, multiple transcription factors predicted to bind to this loci (e.g. IRF4, JUND; RUNX).
Genotyped SNP, in active H3K27Ac mark regulatory region.
This SNP also lies 100 kb upstream of IL20RA and 43 kb downstream of IL22RA2.
In linkage disequilibrium (LD) with genotyped SNP, rs1413088.