Fig. 3From: Clustering of predicted loss-of-function variants in genes linked with monogenic disease can explain incomplete penetranceProportion of genes falling into each cluster, separated by variant class. For each class of variant (synonymous, missense, pLoF), we present the relative proportion of genes where variants of that class were included in each of the six clusters where variants are present. The seventh cluster identifying genes with no variants of a particular class was excluded from the relative proportion calculationsBack to article page