What it is
Variant clinical significance, review status, and protein change.
No sign-in. On for the workspace until you turn the tool off. It does not read your patients.
What it can do
Open ClinVar in the workspace.
No API key and no Connect button. The source is on until someone turns that tool off.
It reads the public record.
NCBI ClinVar.
It is not a diagnosis for a person.
It does not read your patient list, and nothing writes back to a chart or an EHR.
What you can ask
- What germline classification does ClinVar list for this gene?
- What is the review status on this variant?