Hereditary Cancer & Cardiovascular Panel

F24-T2 · DNA Health Blueprint — Clinical Genomics

₹21,000 (PENDING COSTING)Diagnostics only

Given my family history, do I carry an inherited genetic mutation linked to cancer or cardiovascular conditions?

Best for

Strong family history of cancer (especially breast, ovarian, or colorectal) or inherited cardiac conditions, wanting a broader genetic risk picture than F24-T1's cardiac-only panel.

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

BRCA1/2 + 30+ Cancer Genes — Expanded NGS panel for hereditary cancer risk
Cardiomyopathy & Channelopathy Genes — Inherited cardiac condition risk genes
Genetic Counseling — Included — mandatory, part of how genomic results are safely interpreted

What normal doesn't rule out

that you will develop cancer or a cardiac condition — a positive result identifies elevated risk, not certainty, and a negative result doesn't eliminate all risk. Interpreted alongside your family history by a genetic counselor.

Not included

Whole exome sequencing for unexplained conditions (see F24-T3)
Whole genome/longevity sequencing (see F24-T4)

Not the right fit if

your family history doesn't clearly point to hereditary cancer or cardiac conditions specifically — start with F24-T1's more targeted, lower-cost panel first if unsure.

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.

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, including screening recommendations

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: F3 Cancer Risk Evaluation — worth pairing tumour marker screening with genetic risk assessment
Sometimes relevant: F24-T3 Whole Exome Sequencing — if this panel is negative but strong clinical suspicion remains

Other tiers in this family

Cardiac & Pharmacogenomic Panel₹10,000 Clinical Whole Exome Sequencing₹28,000 Whole Genome Sequencing & Longevity Genome₹75,000

If you want more coverage

This tier's price is pending final costing confirmation with our genomics partner. Please confirm current pricing at booking before proceeding.

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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