Heritage Adhoc — Focused cascade testing for families.
HERITAGE · FOCUSED CASCADE TESTING FOR FAMILIES
Heritage Adhoc is a focused test for a specific, already-known variant — the tool for cascade testing. When one family member is found (through Heritage Core or elsewhere) to carry an inherited cancer-risk variant, their blood relatives can be tested precisely for that one change.
One finding can protect many.
A single inherited variant can run through a family. Cascade testing lets relatives learn whether they carry it — so those who do can start earlier screening or prevention, and those who do not can be reassured. It is one of the highest-impact, most cost-effective things a family can do after an inherited variant is found.
How it works
A variant is identified → Relatives are offered testing → A focused test → A plan for each person
Variant is identified
Someone in the family is found to carry a specific inherited variant.
Relatives are offered testing
With their own consent and genetic counselling, blood relatives can be tested.
A focused test
Heritage Adhoc checks precisely for that one known variant — ₹35,000 per member.
A plan for each person
Carriers get a screening/prevention plan; non-carriers get clarity.
Consent & counselling
Every relative makes their own informed choice, supported by KPCIRC genetic counselling.
Every relative makes their own informed choice, supported by KPCIRC genetic counselling. Testing is never imposed, and results are always delivered with support.
TERMINOLOGY ON THIS PAGE
The words you will see, in plain language
Heritage Adhoc is a genomic (DNA-based) test offered for use by qualified healthcare professionals. It is intended to support — not replace — clinical judgement, and must be interpreted alongside your full clinical history, other investigations, and applicable guidelines.
- • A result is not a diagnosis and does not by itself decide treatment.
- • A “not detected” or normal result does not rule out cancer or a genetic change.
- • Not all cancers release enough DNA into blood to be detected.
- • The test does not guarantee access to any medicine, its regulatory approval, insurance cover, or that a therapy will work.
- • Sample-collection kits are for use by qualified phlebotomists only — not for self-testing or self-sampling.
- • Confirmatory testing may be required.
Regulatory status (India). OnKommon's registration of its genomic tests as in-vitro diagnostic (IVD) medical devices with the Central Drugs Standard Control Organisation (CDSCO) is in progress (IVD class pending). Sequencing and variant calling are performed by an accredited laboratory partner (College of American Pathologists — CAP-accredited; ISO 15189) following international guidelines (ACMG/AMP/ASCO/CAP) using a CE-IVD certified variant database. The OnKommon interpretation engine is provided for research and decision-support use. Marketing follows the Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 and applicable Indian advertising standards.
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