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Ionis Familial Chylomicronemia Syndrome (FCS) Testing Program

7 genes

2 - 3 weeks

Notice

The Ionis Familial Chylomicronemia Syndrome (FCS) Sponsored Testing Program with PreventionGenetics will no longer accept samples after October 31, 2026.

To order Familial Chylomicronemia Syndrome (FCS) genetic testing after this date, please:

For questions regarding results interpretation for test completed under this program, a PreventionGenetics representative is available to assist you at support@preventiongenetics.com.

Ionis remains committed to advancing research and supporting the FCS community through ongoing publications in genetic testing and genetic counseling.

Test Criteria

To qualify for the testing program, candidates must reside in the United States or Canada and have evidence of severe refractory hypertriglyceridemia, defined by a minimum of 2 consecutive fasting triglyceride levels > 880 mg/dL or 10 mmol/L in the absence of secondary causes or medical conditions known to cause severe hypertriglyceridemia (sHTG). Informed consent must be provided by the patient.

Specimen(s)

Whole blood, saliva, OCD-100 Buccal Swab

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