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. 2021 May 27;53(1):43–50. doi: 10.1007/s11239-021-02494-4

Fig. 2.

Fig. 2

Association of genetically predicted eGFR with venous thromboembolism using 308 SNPs for eGFR. CI confidence interval, eGFR estimated glomerular filtration rate, IVW inverse-variance weighted, OR odds ratio, SNPs single-nucleotide polymorphisms. There were 10,023 venous thromboembolism cases and 486,809 non-cases in the meta-analysis of IVW-random effects model. Significant heterogeneity was detected among estimates from used SNPs in analyses based on data from both the FinnGen consortium (I2 = 19; Rucker’s Q = 377; phet = 0.004) and UK Biobank study (I2 = 25; Rucker’s Q = 389; phet < 0.001). There was no horizontal pleiotropy in MR-Egger regression using data from FinnGen consortium and UK Biobank study (p > 0.300). One and four outliers were detected in MR-PRESSO analyses using data from FinnGen consortium and UK Biobank study, respectively. However, p values for distortion tests were > 0.05, indicating no significant difference between estimates before and after outlier removing