CGAR

Interactive web application for prioritizing clinically implicated variants via ancestry composition.

What it does

Contextualizes a variant’s clinical significance based explicitly on the patient’s matched population allele frequency background.

STRC usage

Not yet tested on E1659A.

Connections

• STRC Variant c.4976A>C — Misha [see-also]
• STRC Gene [about]
• [part-of] Tools index