Fig. 4From: Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequencesAncestry-specific CF-causing variants characterized. A) Graph of total number of variants (x-axis; Set Size) detected in each ancestry (y-axis). B) Intersection of variants detected across the ancestries. Each column corresponds to the number of variants in each intersection. Ancestries present in each intersection are represented by the black dots. Intersections with single dots represents ancestry-specific CF-causing variants. C) A list of ancestry-specific CF-causing variants. The highest number of unique CF-causing variants (n=50) was detected in EuropeansBack to article page