Additional file 1 of Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunction

Supplementary Material 1. Additional file 1: Table S1.Study characteristics and used software for the four studies used in this meta-analysis. Table S2. Genomic risk loci associated with olfactory dysfunction in model 1 and model 2Table S3. Lead SNPs associated with olfactory dysfunction in model 2. Table S4. Independent SNPs associated with olfactory dysfunction in model 2. Table S5. Genome-wide significant SNPs that are in LD (r2>0.6) with the independent SNPs in model 2. Table S6.ANNOVAR Annotation of the lead SNPs and SNPs that are in LD with lead SNPs in model 2. Table S7. Genes mapped based on positional, Eqtl and chromatin interaction mapping in model 2.Table S8.Chromatin interaction analysis of mapped genes in model 2.Table S9.MAGMA Gene-based analysis in model 2.Table S10.MAGMA Gene set analysis in model 2.Table S11. Functional validation of mapped genes using gene expression analysis.Table S12.PheWAS lookup of lead SNPs.Table S13.Associations between olfactory dysfunction and other phenotypes using individual-level data from the Rhineland Study.Table S14.Two-sample Mendelian Randomization analyses of the effect of olfactory dysfunction on other phenotypes