Fig. 3From: Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associationsRelation between disease prevalence and proportion of the variant database available for filtering. The proposed mode of inheritance is autosomal recessive, the disease prevalence is expressed as 1/n (with n ranging from 1000 to 100,000). Both the variable quantile-based approach and the static 1%-approach are depicted. By definition, for the absence-approach all variants (100%) are available (not shown)Back to article page