Whole Genome Sequencing & Longevity Genome

F24-T4 · DNA Health Blueprint — Clinical Genomics

₹75,000Diagnostics only

Across my entire genome — coding and non-coding regions — what does the most complete genetic picture available reveal about my health and longevity?

Best for

Unexplained conditions after WES, comprehensive longevity/health optimization interest, or anyone wanting the deepest available genomic baseline.

Time at centre: ~15 min blood drawPreparation: None requiredReport: 4–6 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

30x Whole Genome Sequencing — Complete genome coverage, coding and non-coding regions
Pharmacogenomics — How your body metabolizes a broad range of medications
Polygenic Risk Scores — Combines many small genetic effects into a risk estimate for chronic diseases
Genetic Counseling — Included — mandatory, given the scope and complexity of results

What normal doesn't rule out

a deterministic health forecast — polygenic risk scores are probabilistic estimates, not diagnoses, and their clinical utility is still evolving. This is the most comprehensive test available, not a certainty machine.

Not included

Ongoing interpretation as genomic science evolves (a one-time report reflects current knowledge)

Not the right fit if

you haven't tried a more targeted panel first (F24-T1, T2) or WES (F24-T3) — for most specific clinical questions, those are more appropriate and cost-effective than starting here.

Preparation

Preparation: A single blood draw. No fasting or special preparation. || Sample & turnaround: Blood sample, processed by a partnered genomics lab. Turnaround is 4–6 weeks given the scope of full-genome analysis.

Result pathway

Negative

No significant pathogenic findings — polygenic risk scores discussed as probabilistic context

VUS

Variant of uncertain significance — does not automatically establish disease; 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: F25-T2 Full Longevity Profile — pairs naturally with WGS for a comprehensive longevity picture

Other tiers in this family

Cardiac & Pharmacogenomic Panel₹10,000 Hereditary Cancer & Cardiovascular Panel₹21,000 (PENDING COSTING)Clinical Whole Exome Sequencing₹28,000

If you want more coverage

Whole Genome Sequencing is the most complete genomic test in this catalogue — WES and WGS are genuinely different products, not interchangeable.

Genetic counseling is included and mandatory given the scope and complexity of whole genome results — not a separate add-on.

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