Fig. 5: Per SNP Z-score of the novel loci for each of the traits included in the MTAG analysis.

For each novel MTAG loci the lead SNP Z-score of the disease risk allele (beta divided standard error) from all the traits included in each MTAG analysis is represented. SNP identifiers along the x-axis represent the locus number (Supplementary Data 9–11) followed by the genomic position (in GRCh37) and the risk allele. Abbreviations: CV, cardiovascular, other abbreviations and references as per Fig. 1 and Supplementary Data 1.