Begin with Phenotype
Either by starting from a saved file and loading it, or opening the URL, or by entering a new patient, put in the key phenotypic data.
Load the variant table
Use the Load variant file option on the black navigation bar to add genomic information. After a few seconds, it will read out key data on the import. Here, we use a tiny (47-line) public variant file that is laced with the relevant variant. The software loads tens of thousands of variants in a few seconds.
