Whole Exome Sequencing (WES) for Newborns

Whole exome sequencing for newborn genetic screening. Findings require clinical interpretation.

Healthcare professional preparing sample collection equipment beside a seated patient.

AED 3,590

Sample: Blood.
Expected results: 14–30 working days.

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About this test

A newborn genetic screening option listed in the Getchecked Clinic prenatal and genetics catalogue. The card describes assessment of more than 390 genetic conditions that could be relevant to early development and health. A qualified clinician can explain whether this test is appropriate and how to interpret its findings.

What's included

Whole exome sequencing (WES) listed for newborn screening
Assessment covering over 390 genetic conditions, according to the catalogue
Genetic information to support a discussion about appropriate follow-up care

Quick facts

Intended patient: Newborn
Sample: Blood. Confirm collection arrangements with the clinic before booking.
Results: 14–30 working days, as listed on the card
Clinical interpretation: Recommended; screening does not diagnose every condition

Results and included services

Expected results

14–30 working days.

Questions about this test

Who is this test for? The catalogue lists Whole Exome Sequencing (WES) as a screening option for newborns. Confirm suitability with a clinician.

What is assessed? The catalogue describes screening for over 390 genetic conditions relevant to early development and health. Ask the clinic for the exact condition list and limitations.

What sample is needed? Blood. Confirm collection arrangements with Getchecked Clinic before booking.

When are results expected? The card lists 14 to 30 working days.

Do findings provide a diagnosis? Results require clinical interpretation and may call for further assessment or confirmatory testing; screening cannot rule out every genetic condition.