Extended Data Fig. 7: Association analyses of rare coding variants between cases with POI and in-house controls.
From: Landscape of pathogenic mutations in premature ovarian insufficiency

The quantile-quantile plot comparing observed versus expected P values for each rare coding variants in 703 genes (cases n = 1,030, controls n = 5,000, one-sided Fisher’s exact test). The dashed line represents the Bonferroni-corrected P <0.05 threshold. EIF2B2 p.Val85Glu is the only variant that significantly associated with POI.