Virtus Genetics
1800 837 284

Genetic Carrier Screening

Genetic Carrier Screening

Genetic carrier screening looks to identify your risk of having a child with a genetic condition. These conditions can have a significant impact on the child’s health and development. Individuals often have no knowledge that they are carriers of a genetic condition. Carrier screening offers valuable information for family planning, enabling you to make informed choices about pregnancy and your reproductive health. This testing is safe and reliable and can be performed either by blood test or cheek swab in the comfort of your own home.

Thinking about having a baby or already pregnant?

Pre-conception genetic screening allows you to make informed choices as you grow your family.

SELF COLLECT GENETIC TESTING

Our Self Collect Extended Preconception Carrier Screen is coming soon to Virtus Genetics.

Read More >

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SELF COLLECT GENETIC TESTING

Our Self Collect Extended Preconception Carrier Screen is coming soon to Virtus Genetics.

Read More >

Choose your test option

Core carrier screen
Who are the tests for?
Individual carrier status for all tested conditions




Genes
3 genes
Cystic Fibrosis
(CFTR)
Fragile X Syndrome (FMR1)
Spinal Muscular Atrophy
(SMN1)
Genetic ancestry
CFTR testing optimised for European ancestry.
May not be suitable for Asian, Indian, Middle Eastern or other ancestries
Testing location
Australia - (Virtus Genetics)
Price Out of Pocket after Medicare Rebate
Bulk Billed
Initial Price Upfront and Non Medicare Patients
Non Medicare eligible fee
$400 per person
Core + carrier screen
Who are the tests for?
Individual carrier status for all tested conditions


Genes
6 genes
Cystic Fibrosis
(CFTR)
Fragile X Syndrome (FMR1)
Spinal Muscular Atrophy
(SMN1)
Alpha and Beta thalassemia
(HBA1/HBA2 and HBB)
Genetic ancestry
Suitable for all ancestries





Testing location
Australia - (Virtus Genetics)
Price Out of Pocket after Medicare Rebate
Out of pocket $230 per
person




Initial Price Upfront and Non Medicare Patients
Upfront and Non Medicare
Fee $570 per person
Medicare rebate available
based on eligibility
$340 Medicare rebate
available for eligible
patients.
Duo carrier screen
Who are the tests for?
Couple carrier status for all tested conditions
Genes
Up to 390 genes
• Couple specific - repeat
carrier screening required
if reproductive partner
changes
• Cannot be used with
donated eggs or sperm
Genetic ancestry
Suitable for all ancestries


Testing location
Australia - (Virtus Genetics)
Price Out of Pocket after Medicare Rebate
Out of pocket $650 per
couple




Initial Price Upfront and Non Medicare Patients
Upfront and Non Medicare
fee $990 per couple.
($475 per person)
Medicare rebate available
based on eligibility
For non-Medicare eligible
patients total fee is $990
Individual Expanded Carrier Screen
Who are the tests for?
Comprehensive individual carrier status for all tested conditions. Recommended for patients
using egg or sperm donors or patients wanting to know their individual carrier status
Genes
Option 1
Legacy ECS
- Male individuals (268 genes)
- Female individuals (289 genes
+ additional X-linked genes)
Option 2
700+ Fulgent Expanded
Carrier Screen
Genetic ancestry
Suitable for all ancestries





Testing location
United States - (Fulgent)
Price Out of Pocket after Medicare Rebate
Legacy ECS
$790 per person* 
700+ Fulgent Expanded Carrier Screen $999 per person*
*Please note that no medicare
rebate available for this testing
Initial Price Upfront and Non Medicare Patients
Legacy ECS
$790 per person*
700+ Fulgent Expanded
Carrier Screen
$999 per person*
*Please note that no medicare
rebate available for this testing


* Your specimens and personal information will be made available to Fulgent for the purposes of providing test services and performing related activities, as further described in
Fulgent’s Privacy Policy (www.fulgentgenetics.com/policies/privacy-policy).
# Private billing charges will apply in the case of Medicare rejections.

Unsure which test is right for you?

Email [email protected] or call 1800 837 284.

For more information on the tests, download our brochures below.

Download

Select a link below to download the appropriate test information.
Duo
Duo Carrier Screen Genes List
Genetic Carrier Screen

Genetic Carrier Screening FAQ’s

Why should I consider Carrier Screening if I have no family history?

Individuals often have no knowledge that they are carriers of a genetic condition. Carriers will have one healthy copy of the gene that works well enough to prevent them from developing symptoms of the condition. In contrast, children affected by these conditions have no working copies of the gene. Inheritance of these genetic conditions can happen in two main ways: Autosomal recessive and X-linked inheritance.

Autosomal recessive conditions: If both the male and female individuals are found to be carriers of a variant in the same gene, there is a 1 in 4 (25%) chance of having a child affected by that genetic condition. Most of the screened conditions are autosomal recessive.

X-linked conditions: Female carriers of an X-linked condition (caused by a gene on the X chromosome) have up to a 1 in 2 (50%) chance of having a child affected by that genetic condition, irrespective of the male reproductive partner’s carrier status.
Genetic Carrier Screens

Who should be screened?

Genetic Carrier screening may be suitable regardless of your family history, genetic ancestry, or age. Most children born with a genetic condition will not have a family history of the condition. Nevertheless, if you are aware of a family history of a genetic condition, it is important to discuss this with your doctor.

Unlike chromosomal conditions (e.g., Down syndrome) that occur more commonly with advanced maternal age, the risk of being a carrier of a genetic condition does not vary with age. We are born with our genetic variants, usually inherited from our parents, and these do not change over time.

When should we be screened?

The ideal time for reproductive carrier screening is when planning a pregnancy. Screening before becoming pregnant gives couples the widest array of reproductive options. Genetic Carrier screening is also commonly used in early pregnancy.

How will these results help my partner and I when planning a family?

Genetic Carrier screening results will inform your reproductive decision making. Couples identified as being at high risk of having a child with a genetic condition will have the option of screening embryos with preimplantation genetic testing (PGT) before pregnancy, or the option of testing a baby during pregnancy. Having this information allows couples to make reproductive choices right for them to ensure they have the highest chance of having a healthy family.

Virtus Genetics is a leading provider of PGT in Australia. A Medicare rebate for PGT is now also available for couples at risk of having children affected by a genetic condition.

Watch the video below to learn more about genetic carrier screening and how genetic conditions are inherited.

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