Cohort insights

These figures summarise the variation in the Enigma Clinical Platform release as a whole: what kinds of variants it holds, how they are classified in ClinVar, how many have not been seen in gnomAD, how common they are, which genes carry the most, and which phenotypes are recorded. They are counted directly from the cohort database and refreshed daily.

Only aggregate counts are shown. Counts of individuals below 5 are withheld, and no sample identifiers are ever sent to the browser. Every table can be exported.