Phenotype Matching

In VarSome Clinical you can add known phenotypes or diseases linked to the sample you analyze. In the "Launch analysis" page you can start typing a phenotype or a disease according to HPO in the respective field and include this information when launching a new analysis.


In the Variant Table, a column named Phenotypes (or Diseases) will be visible and for each variant reported, it will include the number of phenotypes or diseases linked to the gene including the variant and matched to the phenotypes or diseases provided when launching an analysis. Then, you can sort by that column to prioritize variants accordingly.