No products in your basket.
Purchase your test with
Price range: £385.00 through £899.00
The Ventrilia cardiovascular genetic test checks selected genes linked to inherited heart and blood-vessel conditions. You can choose from seven focused panels for defined clinical areas or a broader panel covering 292 genes across the cardiovascular range.
Ventrilia can add a genetic perspective when you are trying to understand an inherited heart concern or a pattern within your family. Through My DNA Lab, you can access this testing privately and use the report to support an informed conversation with your GP, cardiologist or inherited cardiac conditions specialist.
Your kit includes a Buccal Cheek Swab and clear instructions, allowing you to collect your sample from the comfort of home. Once your sample is ready, contact us and we will arrange collection from your home.
Some heart and blood-vessel conditions are linked to inherited gene changes. Ventrilia therefore includes focused panels for aortic conditions, heart rhythm conditions, heart muscle conditions, heart conditions present from birth, inherited high cholesterol, pulmonary hypertension and RASopathies. The broader option brings together 292 genes from across these clinical areas.
Because each panel asks a different genetic question, review the Ventrilia panel list as well as the full gene list before choosing. Both resources are available under ‘Test provider and further information’ further down this page.
Ventrilia is a focused medical test rather than a general heart wellness check. Its findings become more useful when they are considered alongside symptoms, family history, examination, ECGs, scans, cholesterol results and other relevant investigations.
Ventrilia may suit you when an inherited heart or blood-vessel condition is suspected or has already been diagnosed. It may also be relevant if your family history includes an inherited heart condition or sudden cardiac death, or if a heart specialist has recommended genetic testing.
If a genetic change has already been identified in your family, a focused test designed to look for that change may be more useful than a new broad panel. If you arrange pre-test genetic counselling, you can decide whether to discuss the existing family report during that session.
Fainting, a seizure, chest pain, severe breathlessness or another urgent symptom needs prompt medical assessment. Do not wait for a private genetic test or result.
Your report may identify a gene change that could help explain an inherited heart condition, find no relevant change or identify a change that is not yet fully understood. Each outcome needs to be considered in the context of the clinical question.
A significant finding may help a heart specialist plan further checks or decide whether biological relatives should be offered focused testing. However, a negative result cannot rule out an inherited condition, particularly when symptoms or family history remain concerning.
The provider states that carrier status is not reported for recessive conditions. It also explains that an uncertain finding may be reviewed again as scientific knowledge develops, so any later update should still be interpreted alongside your clinical information.
We always recommend that you discuss your results with your healthcare professional. Do not start or stop heart medication, change exercise restrictions or alter follow-up from the report alone. Share the complete report with your GP or heart specialist.
When a cardiologist has identified a likely clinical area, the matching focused panel may provide the clearest starting point. Rhythm, heart muscle and aortic conditions involve different groups of genes and different follow-up. The broader option covers more genes, but more information is not automatically more useful.
If no diagnosis has been made, a heart assessment can help clarify which genetic question needs to be asked. For example, an ECG, scan, cholesterol test or another investigation may point towards the most relevant panel.
A significant result may also matter to biological relatives by supporting focused family testing or conversations about monitoring. Equally, a negative result may not remove the need for follow-up when symptoms or family history remain concerning.
Bring previous ECGs, scans, cholesterol results and family genetic reports to the professional reviewing your result. Together, these records provide the context needed to understand whether the genetic finding is relevant.
