Anne and Heidi suggested making it more obvious that the automated/preliminary estimates are not manually reviewed. To accomplish this we can make a few changes.
1) Rename the column to "Preliminary genetic prevalence estimates (ClinVar LP/P and gnomAD HC LoF)"
2) Add a hover over saying "Preliminary genetic prevalence estimates are algorithmically generated using ClinVar pathogenic/likely pathogenic variants and gnomAD high confidence predicted loss-of-function variants only. These estimates have not been manually reviewed and may contain non-disease causing variants. Use with caution."
3) On the estimate page update the note at the top to say "This list was algorithmically generated for the gene [GENE], with the transcript {TRANSCRIPT]. This algorithm uses ClinVar pathogenic/likely pathogenic variants and gnomAD high confidence predicted loss-of-function variants only. These estimates have not been manually reviewed and may contain non-disease causing variants. Use with caution."
Anne and Heidi suggested making it more obvious that the automated/preliminary estimates are not manually reviewed. To accomplish this we can make a few changes.
1) Rename the column to "Preliminary genetic prevalence estimates (ClinVar LP/P and gnomAD HC LoF)"
2) Add a hover over saying "Preliminary genetic prevalence estimates are algorithmically generated using ClinVar pathogenic/likely pathogenic variants and gnomAD high confidence predicted loss-of-function variants only. These estimates have not been manually reviewed and may contain non-disease causing variants. Use with caution."
3) On the estimate page update the note at the top to say "This list was algorithmically generated for the gene [GENE], with the transcript {TRANSCRIPT]. This algorithm uses ClinVar pathogenic/likely pathogenic variants and gnomAD high confidence predicted loss-of-function variants only. These estimates have not been manually reviewed and may contain non-disease causing variants. Use with caution."