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. Author manuscript; available in PMC: 2024 May 30.
Published in final edited form as: Twin Res Hum Genet. 2024 Apr 22;27(2):69–79. doi: 10.1017/thg.2024.19

Figure 3.

Figure 3.

The associations between PGSDBP, PGSDBP_GC and disease phenotypes in individuals with primarily European ancestry (n = 66,482).

Note: Panel A, PheWAS for PGSDBP. Panel B, PGSDBP_GC. Associations for 1322 phenotypes are shown. On the x-axis, the phenotypes clustered according to broad phenotypes represented by different colors. P values are shown on the y-axis, with upturned triangles representing positive associations and downturned triangles representing negative associations. The five phenotypes with the smallest p values are labeled; however, none of phenotypes exceeded the Bonferroni multiple testing threshold (p < 3.78e-05). In Panel B, Vitamin D deficiency is also labeled for reference. Full details are provided in Supplementary Data 3 and 5.