CGAR

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

Key Info

• URL: https://cgar.org/
• Category: Clinical
• API: Limited
• Free: Free
• ACMG Relevance: PM2, PS4
• Link Status: Unchecked

Why It Matters

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

STRC Research Usage

Not yet tested on E1659A.

Next Steps

• Verify URL accessibility
• Test with STRC E1659A variant if applicable
• Document specific results

Connections

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