Free Genetic Counselling for your heart■

Worried About Your Heart Health?
Get a Free Genetic Risk Assessment Today

Uncover hidden risks of inherited heart conditions—before symptoms begin. This one-time test uses advanced DNA technology to give you clarity, control, and peace of mind about your cardiac future. This test includes a free expert counselling session to help you understand your results.

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Cardio Screening

Comprehensive genetic information on inherited heart disorders

Genetic Test for Inherited Heart Disease■

Let’s uncomplicate your heart health

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An NGS-based test for identifying genetic risk factors associated with developing inherited heart disorders.
  • Informed diagnosis and management
  • Comprehensive information on genetic variants
  • Early detection and risk prediction

Inherited Heart Conditions We Test For

Cardiomyopathies
Cardiomyopathies
Conditions affecting the heart muscle
Channelopathies
Channelopathies
Conditions affecting electrical signalling
Aortopathies
Aortopathies
Conditions affecting aortic blood flow
Familial Cholesterolemia
Familial Cholesterolemia
Conditions affecting cholesterol metabolism
Rare Diseases
Rare Diseases
Uncommon diseases affecting heart function

Who Should Get Tested?

Essential for:
ALL
Especially for Patients with:
✦ Family history of sudden cardiac death
✦ Clinical diagnosis of cardiomyopathies
✦ Suspected genetic heart diseases
✦ Inherited heart conditions
✦ At-risk family members
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Benefits

Benefits of DGx Cardio Genetic Screening

  • Identifies genetic risk associated with heart health
  • Personalizes treatment and management for identified patients
  • Enables proactive steps for optimal heart health
  • Prevents adverse cardiac events

What Makes DGx Cardio Screening Different?

  • High quality genetic analysis and results
  • Up-to-date on the latest variant database and guidelines
  • Actionable and easy-to-interpret report
  • Reliable customer support available throughout the process
Benefits

DGx Cardio Screening — Test Specifications

Specimen required:
1-2ml EDTA-Blood
Specimen required:
Sequencing coverage:
>99.0% >20X
Sequencing coverage:
No. of genes covered:
78
No. of genes covered:
Variant types covered:
SNPs, indels
Variant types covered:
Turnaround time:
28 Days
Turnaround time:
Guidelines followed:
ACMG guidelines
Guidelines followed: