Newborn Carrier Testing by BioGeneticsRx.com

Your patient is interested in discussing newborn genetic testing with you. Below is some information for you in regards to Cquentia Newborn Test and how to provide this service to your patient.

DON’T RISK IT...SCREEN IT!!!

The Power of Diagnostics at the Speed and Price of a Screen

What is the Cquentia Newborn Test?

A genomics-based, multiple-gene panel that identifies pathogenic mutations potentially responsible for disease presentation.

What genes are on the panel?

There are 92 genes clinically tied to conditions identified on the American College of Genetics (ACMG) Recommended Uniform Screening Panel (RUSP) (see reverse side for details).

How can I use this test?

There are three indications for using the Cquentia Newborn Testing Panel:

Diagnostic/Reflex test for Abnormal Screening Results
Supplemental Newborn Screening
Carrier/Family Planning Screening

What information does this screening provide?

Reports include all clinically significant variants identified within the targeted genomic regions. In addition Variants of Unknown Significance (VOUS) are reported for future use and interpretation.

For more information please contact BioGeneticsRx to schedule an appointment with a Representative

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