DNA Test

Mygenia ONE Carrier Screening Panel

34 items


The ONE You Needed To Identify The Risks In Your Health Condition. Mygenia ONE CARRIER Screening Panel uses the Next Generation Sequencing Technology (NGS). The technology can screen for numerous gene by simply taking only 6ml of blood samples , able to test more than 1000 Genetic Diseases for you.

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Full Description

pangenia introduction

Why do I need to do genetic disease health risk assessment?
Even though our generation has been very concerned about health by maintaining healthy lifestyle and eating habits, however, we cannot choose our genes since this is inherited from our parents. Parent is play an important role for caring and planning for their children's health and future. If the couples are carrier of a disordered gene, their children still have the risk of suffering from the genetic disorders even if the couples do not have symptoms of the disease. If the genetic disease has not been found at an early stage, this may lead to a severe diseases which is difficult to cure and cause a serious impact on daily life.

Mygenia ONE CARRIER Screening Panel uses the Next Generation Sequencing Technology (NGS).
The technology can screen for numerous gene by simply taking only 6ml of blood samples , able to test more than 1000 Genetic Diseases for you. Whether there is a high risk of inherited diseases, you can understand about the physical condition in the earlier stage, and take the appropriately prevention.

DNA Increased awareness
If you know you have a genetic risk for a disease you’re likely to be vigilant in protecting your health and being aware of the warning signs of something more serious.

Time to take preventative measures
You are more likely to tread with caution and take measures that may mitigate your condition. For example, changes in lifestyle and diet, regular check-ups and doctor visits.

Preparing the next generation
Looking after your loved ones and preparing them for the future is important, especially when it comes to health. If both parents are carriers of a condition but have not exhibited symptoms themselves, their children may still be at risk of inheriting the condition

Identifying rare diseases
Many unusual symptoms and abnormalities can be difficult to diagnose. For example newborn babies are unable to communicate their symptoms. A hereditary risk assessment can help doctors diagnose an infant’s condition soon after birth.

We help to identify the risk of inherited genetic disorders, so you can prepare and protect yourself for the future. You and your doctor can identify avenues for more effective treatments and medicines.

Medical consultation is included without additional charge
- Free interpretation of test reports, analysis of genetic disease risk.
- Free assessment of the family's risk of the same genetic gene (if applicable)

4 Advantages

Advanced technology
We provide access to the latest in molecular diagnostic testing via the most advanced available technology for genetic screening and hereditary risk assessments.

Efficient results
Every minute counts when it comes to health,. Our fast turnaround times get you the comprehensive DNA data, results and analyses you need, quickly and efficiently.

Expert analysis
We provide in-depth data analysis, specialist knowledge and valuable insights that enable you to provide the best possible care, recommendations and courses of treatment.

Consulting specialists
To complement our in-house expertise, we work closely with consulting specialist, Dr. Christopher Corless, to provide additional advice and analysis. An expert in surgical pathology and molecular diagnostics, Dr. Corless works from our partner lab, Knight Diagnostic Laboratories, a US-based global leader in genetic testing for solid tumours and hematopoietic malignancies.

pangenia order flow

Only 6ml blood sample is required for the genetic screening. Customer has sample collected in the listed clinics or at Pangenia office. The clinic will contact Customer to schedule report explanation by doctor after receiving the report from Pangenia. Alternatively, customer may receive the report by mail and call Pangenia hotline for inquiry about the result. Pangenia can also refer Customer to specified doctor/genetic counsellor to follow up.

Recommended for

- Having family history of genetic disease
- Couples who planning for marriage or having family planning
- Worry about yourself is carrier
- Anyone with all ages who wants to identify the genetic disease risk

Special Promotion

- Each customer will entitle $200 PARKnSHOP Cash Voucher!  First-come-first-served while stocks last.

Common genetic disorders
  • Alpha-Thalassemia
  • Beta-Thalassemia
  • Cystic Fibrosis
  • Spinal muscular atrophy
  • Duchenne muscular dystrophy
  • Smith-Lemli-Opitz syndrome
  • X-linked adrenoleukodystrophy
  • 3-Phosphoglycerate Dehydrogenase Deficiency
  • Abetalipoproteinemia
  • Alport Syndrome
  • Autism Spectrum
  • Epilepsy
  • Arthrogryposis
  • Bardet-Biedl Syndrome
  • Beta-Hemoglobinopathies
  • Bloom Syndrome
  • Canavan Disease
  • Carnitine Palmitoyltransferase II Deficiency
  • Congenital Amegakaryocytic Thrombocytopenia
  • Congenital Disorder of Glycosylation, Type 1A, PMM2-Related
  • Dyskeratosis Congenita
  • Familial Dysautonomia
  • Familial Hyperinsulinism
  • Fanconi Anemia
  • Joubert Syndrome 2
  • Gaucher Disease
  • Mucolipidosis
  • Niemann-Pick Disease
  • Polycystic Kidney Disease, Autosomal Recessive
  • Retinitis Pigmentosa
  • Tay-Sachs Disease
  • Tyrosinemia
  • Usher Syndrome
  • Wilson Disease
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  • $200 Park N Shop Gift Coupon
Terms & Conditions
Terms and conditions of ordering the Mygenia assessment:

After successful payment, the Customer receives confirmation email from ESDlife. Pangenia will call the Customer to schedule the appointment within 1-3 working days. Customers can also arrange appointment by calling 39897211 after payment.


There are two options for the Customer:


  1.      Customer has sample collected directly at Pangenia, where the sample will be analyzed. The report will be mailed to the address provided by the Customer. Customer may call Pangenia hotline for inquiry about the result. Pangenia is willing to refer Customer to specified doctor/genetic counsellor to follow up.


  1.      Customer has sample collected in the listed clinics or at Pangenia office. The samples will be delivered to Pangenia for analysis. The clinic will contact Customer to schedule report explanation by doctor after receiving the report from Pangenia.


Customers must present their identity cards and the printed order confirmation letter on the appointment day.


Customers who purchase the Mygenia Hereditary screening with discounted price for 2 persons must present their DNA samples at the same day. Post-test consultation will be carried out for 2 persons at the same day. 


The package is valid for 3 months (from the date of purchase) or it will be forfeited.


Report will be ready around 6 weeks and interpreted by medical and genetic professionals.


Amendment or cancellation is not allowed once the payment is confirmed.


The package cannot be transferred to a third party.


All tests are not for the purpose of medical diagnosis or treatment.


In case of dispute, ESDlife and Pangenia Lifesciences Limited reserve the right to make the final decision.


Disclaimer: ESDlife does not operate or provide the service above. ESDlife is irresponsible to any loss, injury or law action caused by using this plan. Any claims and inquiries should be addressed to Pangenia Lifesciences Limited.


Locations for sample collection:

1. Pangenia Lifesciences Ltd.

Floor 28, Tower A, Billion Centre, 1 Wang Kwong Road, Kowloon Bay, Hong Kong


2. Premier Clinic

19/F, Asia Standard Tower, 59 Queen's Road, Central, Hong Kong


3. Specialist in Family Medicine

3A, Shinyam Commercial Building, 163 Johnston Road, Wanchai, Hong Kong


Are you really as healthy as you think?

You may look healthy and fine today that serious diseases seem to be far away from you. However, have you ever thought that threatening diseases are lurking deep within your body?


Genes inherited from the previous generation, not only will affect your physical appearance, but also secretly buried a lot of risk factors for your health status.Nowadays scientific researches confirmed that many diseases are actually related to your genes, such as cancer and sudden death caused by heart diseases.


However, the incidence of genetic diseases can actually be effectively reduced by proper precautions. An early understanding of your own genes can keep you away from genetic diseases.


Who should be assessed?

Pangenia recommends that all people should be assessed, especially those with family history of genetic diseases. People who worry that they will suffer from genetic diseases should carry out a comprehensive health assessment of the genes. Genetic diseases are often hidden, but they can trigger life-threatening situations in a sudden. Therefore, you are advised to take preventive measures early to understand your genetic status.


What is Mygenia ONE? Is it reliable?

The Mygenia ONE Health Risk Assessment examines the state of genes associated with inherited diseases in your blood sample using a new generation of gene sequencing technology.


Pangenia professional team looks at your genetic information and refers to an internationally recognized gene database to determine if your gene has pathogenic variations and report to you.


Mygenia ONE uses the most advanced new-generation gene sequencer in Hong Kong to process the test for you. The PANGENIA scientific team is trustworthy that 30 % of the professionals have a doctorate in addition to the medical laboratory technician recognized qualifications.


What will I get after the test?

After detailed analysis of the relevant genes, Pangenia team of professional laboratory technicians will report your gene profile based on the latest gene database, and list out the relationship between the gene variations and the related diseases. Your doctor can help you choose the most appropriate precautions.


How long is my report valid?

Genetic variations remain unchanged throughout your lifetime. In addition, we will provide you with a report review service to ensure the maximum protection for you. As long as you have received a Mygenia ONE health risk assessment, you can apply for periodic updates to your report. Our scientific team will update you on the latest information about the diseases and the corresponding genes in the genetic database. As a result, your reports will continue to be valid.


How should I conduct the test?

Please contact and consult your doctor first. Your doctor will take 6 ml of blood, along with the completed test application form and then send it to PANGENIA's laboratory for testing. You will receive your report within 6 weeks.


Health Risk Assessment of Inherited Diseases

Why do I need to do genetic disease health risk assessment?

Although our generation is very concern about healthy life style and eating habits, we cannot choose the genes inherited from previous generation. And as parents, caring and planning the future health of our children play an important role. If both husband and wife are carriers of a defected gene, even though they do not have apparent symptoms, their children may still suffer from genetic diseases. Without early detection, we may ignore the serious diseases that they cannot be cured afterwards.


How does genetic disease health risk assessment help me?

Genetic disorders can seriously affect your daily lives. Mygenia ONE genetic disease health risk assessment screens multiple genes using Next Generation Sequencing (NGS). The test only needs 6 ml of blood sample, and can examine more than 1,000 genetic diseases to assess whether you have a high risk of inherited diseases, allowing you to get a better understanding of your physical condition and take appropriate precautions.


The Mygenia CARRIER genetic disease health risk assessment covers the most common genetic disorders as follow:


Spinal Muscular Atrophy (SMA)

Ankylosing spondylitis (AS)

Insulin-dependent diabetes mellitus (IDDM)


Congenital Glaucoma

and many more


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