If I'm in a gene and select a variant that is not in the list of prioritized variants at the left, I can still mark this as Significant, but:
The badge under findings only counts the variants in the left bar,
The variant I just added cannot be easily discovered again as it isn't in the left menu
As a result, if I mark up any variants that were not originally found, they will be immediately lost. We might want to discuss how we want to fix this, but we could:
Put the annotated variant in the reviewed category
Update the badge to reflect the number of observed pathogenic variants
Update the number of Variants under Review Variants to include this variant
If the significance is set to Not significant, it would be removed from the Reviewed category, and will not be put into any other category. That is probably fine, but we could consider creating a new category to house reviewed variants that aren't important.
If I'm in a gene and select a variant that is not in the list of prioritized variants at the left, I can still mark this as Significant, but:
As a result, if I mark up any variants that were not originally found, they will be immediately lost. We might want to discuss how we want to fix this, but we could:
If the significance is set to Not significant, it would be removed from the Reviewed category, and will not be put into any other category. That is probably fine, but we could consider creating a new category to house reviewed variants that aren't important.