Briefly describe the feature and provide meaningful references
select-clinVar-submissions.R should be modified to remove the criterion where, if a P/LP submission has an associated phenotype, it is selected over other conflicting submissions.
What input data are required for this feature or analysis?
ClinVar variant and submission summary files
How do you plan to organise the feature or analysis - will it be a multi-function call or add to existing functions?
Will modify select-clinVar-submissions.R
Who will complete the feature request (please add a GitHub handle here if relevant)?
Purpose/implementation Section
Briefly describe the feature and provide meaningful references
select-clinVar-submissions.Rshould be modified to remove the criterion where, if a P/LP submission has an associated phenotype, it is selected over other conflicting submissions.What input data are required for this feature or analysis?
ClinVar variant and submission summary files
How do you plan to organise the feature or analysis - will it be a multi-function call or add to existing functions?
Will modify
select-clinVar-submissions.RWho will complete the feature request (please add a GitHub handle here if relevant)?
@rjcorb