myHealthScore - Veritas

Veritas

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Description

myHealthScore is a genetic test that provides information about a patient’s risk of common multifactorial diseases. The test analyzes polygenic risk providing detection for a larger number of people.

260€

PURCHASE MYHEALTHSCORE

What is polygenic risk?

The most common diseases are often multifactorial in origin meaning that they are caused by the effect of genetics together with other factors such as lifestyle and environment.



Knowing the patient’s genetic risk for specific diseases allows for the development of prevention plan based on related modifiable risk factors.

The most common diseases are often multifactorial in origin meaning that they are caused by the effect of genetics together with other factors such as lifestyle and environment.

Which diseases are included in myHealthScore?

Cardiovascular disease*

>2 millions variants

Type 2 diabetes

> 600,000 variants

Breast cancer

> 550,000 variants

Prostate cancer

> 650,000 variants

myHealthScore is available for cardiovascular disease, type 2 diabetes and cancer risk either separately or together.

*For a more comprehensive analysis of cardiovascular disease, the test includes the polygenic risk of: coronary artery disease, atrial fibrillation, lipid profile (triglycerides, LDL and HDL cholesterol) and hypertension.

Purchase myHealthScore

260€

Includes

Cardiovascular disease analysis
Breast cancer and prostate cancer analysis data
Type 2 Diabetes analysis
PURCHASE MYHEALTHSCORE

myHealthScore includes

  • Whole genome sequencing technology and analysis with CE-IVD software.
  • Analysis of thousands to millions of variants related to the conditions tested.
  • Possibility of extending the assay to other conditions as the science advances.
  • Access to Veritas calculator to assess the absolute risk based on genetic and clinical factors.

How do I start?

1. Acquire your kit and receive the pre-test genetic counselling consultation

Once you have purchased the test, we will contact you to schedule a genetic counselling consultation to understand your personal and family history and prescribe the test.

1. Receive your kit, collect your sample and request the shipment

You will receive a kit for saliva sample collection. Once the sample is ready, we will send a courier to collect the kit.

3. We analyse your sample and provide the test result

We sequence your DNA, analysing the relevant clinical information to issue your report, which will be ready in 4 weeks.

4. Delivery of results

Results are provided that will be used to support the medical care of the patient.