Genetic Testing for Monogenic Diseases — 200+ Gene Panel

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Genetic Testing for Monogenic Diseases — 200+ Gene Panel
A comprehensive genetic test that screens for monogenic diseases — conditions caused by a change in a single gene. Using targeted sequencing of biologically relevant variants across 200+ genes, this panel provides broad, in-depth screening for inherited disorders.
Key details:

Screens for a wide range of monogenic (single-gene) diseases
Covers conditions across 10 body systems
Targeted sequencing focused on the variants that matter most
Simple 5 cc blood sample
Results emailed within 15–35 business days

This test is especially valuable for individuals managing a rare genetic disorder, or those with a family history of monogenic disease who want comprehensive insight into their genetic health.

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