Cardiac & Pharmacogenomic Panel

F24-T1 · DNA Health Blueprint — Clinical Genomics

₹10,000Diagnostics only

Do I carry an inherited genetic risk for cardiac conditions, and how might my body process common medications differently?

Best for

Family history of inherited cardiac conditions (cardiomyopathy, arrhythmia syndromes), or anyone wanting pharmacogenomic guidance before starting long-term medications.

Time at centre: ~15 min blood drawPreparation: None requiredReport: 2–3 weeks (partnered lab)Booking: Self-bookCollection: Blood: Home* or Centre

Before you book — please read: Eligibility for this package is screening information only. Metal implants, pacemakers, claustrophobia, age, or risk profile may apply. This does not block booking — our clinical team confirms eligibility in person at your visit.

What's included

Inherited Cardiac Risk Genes — Screens for genes linked to cardiomyopathy and arrhythmia syndromes
Pharmacogenomic Panel — How your body metabolizes common medications, e.g. statins and blood thinners
Genetic Counseling — Included — mandatory, part of how genomic results are safely interpreted

What normal doesn't rule out

that you will or won't develop a cardiac condition — genetic risk is probabilistic, not deterministic, and needs interpretation alongside your family history and clinical picture by a genetic counselor.

Not included

Hereditary cancer genes (see F24-T2)
Broader genome sequencing (see F24-T3, F24-T4)

Not the right fit if

you're looking for hereditary cancer risk specifically — see F24-T2 instead, which is purpose-built for that.

Preparation

Preparation: A single blood draw. No fasting or special preparation. || Sample & turnaround: Blood sample, processed by a partnered genomics lab. Turnaround is 2–3 weeks — longer than routine diagnostics, since this involves specialized sequencing and interpretation.

Result pathway

Negative

No pathogenic variant found — interpreted in context of your family history with your counselor

VUS

Variant of uncertain significance — does not automatically establish disease risk; explained by your counselor

Pathogenic

Genetic counseling and clinical management pathway discussed directly

Family implications

A pathogenic finding may have implications for blood relatives — discussed during counseling

Clinically relevant

Add-ons matched to this package — not “frequently bought”.

Strongly relevant: F22 TriScan — a structural cardiac calcium score pairs naturally with inherited cardiac risk genetics
Sometimes relevant: F24-T2 Hereditary Cancer Panel — if family history also includes cancer

Other tiers in this family

Hereditary Cancer & Cardiovascular Panel₹21,000 (PENDING COSTING)Clinical Whole Exome Sequencing₹28,000 Whole Genome Sequencing & Longevity Genome₹75,000

If you want more coverage

A genetic counselor can help you choose — or book directly if you already know what you need. Genetic counseling is included with every F24 tier regardless.

Genetic counseling is included and mandatory for every tier of F24 — not a separate add-on, but part of how results are safely delivered and interpreted.

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