Update scope of manual variants to include unnanotated variants in seqr #5181
Description
Is your feature request related to a problem? Please describe.
Certain variants in seqr, for example, that are not associated with a gene, lead to issues with reporting. So far we've been creating manual variants, but we'd like to brainstorm better ways to approach it.
Describe the solution you'd like
Update scope of manual variants to include unnanotated variants in seqr. It would be useful to have a list of manually created variants so can capture all use cases.
Describe alternatives you've considered
NA
Additional context
NA