Selecting a Variant
SOP Section 5.1
Last updated
SOP Section 5.1
Last updated
Before selecting a variant, confirm you are logged in to the desired Affiliation. For assistance, see Affiliations.
Select “New Variant Curation” in the top right of the interface.
Enter the Variant ID using either the ClinVar Variation ID or the ClinGen Allele Registry ID; please note the Allele Registry allows for novel variants to be registered by users.
Click "Retrieve" and confirm that it is the correct variant.
Then select "View Evidence" to enter Evidence View.
You will now enter Evidence View.
If you had previously begun an interpretation for this variant, you will be taken directly to Interpretation mode. You may have one interpretation per variant per dashboard.
