Additional file 1 of Integrating plasma proteomes with genome-wide association data for causal protein identification in multiple myeloma

Additional file 1: Table S1. Detailed information for data source of confounders used in the current study. Table S2. Genetic variants for Mendelian randomization analysis of the associations between causal risk proteins and multiple myeloma. Table S3. Mendelian randomization results of causal risk proteins on multiple myeloma. Table S4. Information of genetic variants for MR-BMA analysis. Table S5. Test of influential genetic variants in MR-BMA. Table S6. Test of outlying genetic variants in MR-BMA. Table S7. Top 10 models ranked by the model posterior probability after model diagnostics. Table S8. Meta-analysis for the effect of genetically predicted causal risk proteins on the risk of MM from FinnGen and UK Biobank. Table S9. Genetic variants for Mendelian randomisation analysis of the associations between multiple myeloma and significant proteins. Table S10. Mendelian randomization results of multiple myeloma on significant proteins. Table S11. Mendelian randomization of blood proteins on multiple myeloma using only variants in the cis-region of the gene encoding the blood proteins.