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Going through a genetic report as a family | CION Cancer Clinics

A genetic report changes what a whole family needs to think about, not just the person tested, and it rarely makes sense on a single reading. Here are the different ways families choose to share it, how to start the conversation at home, and what a counsellor can do to help. At CION Cancer Clinics in Hyderabad, our oncologists review your family history with you and guide you to the right genetic counselling and testing.

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Medically reviewed by Dr. Naresh GunduConsultant Medical Oncologist · MBBS, DNB (Internal Medicine), DM (Medical Oncology, AIIMS) · last reviewed September 2026, next review due September 2027
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The short answer

How should a family go through a genetic report together?

Slowly, and usually more than once. A genetic report changes what a family needs to think about, not just the person who was tested, and it rarely makes sense on a single reading. Most families do better bringing it to a counselling session together than passing round a photograph of the page on a phone.

Why one person reading it alone is not enough

The person who was tested often hears the result under stress, at the same appointment as other news. Details get missed, and the version retold to relatives afterward can drift from what the report actually says. A joint session, or at least a shared written summary, keeps everyone working from the same facts, rather than several slightly different retellings circulating around the same family.

Who actually needs to be in the room

There is no fixed rule. Some families bring everyone at once. Others prefer the person tested hears it first, alone, and chooses how and when to bring in the rest. Either approach is reasonable, as long as the facts that reach relatives are accurate and nobody is left working from an incomplete or secondhand version.

A counsellor can meet with the whole family together if that is what feels right. This is a normal request, not an unusual one.

Different families, different pace

Ways families choose to share a result

None of these is the "correct" way. Choose what fits how your family already talks.

Everyone together, from the start

The whole family hears the result at once, often in one counselling session, so nobody is retelling it secondhand. It works best in families that already talk openly about health.

One person first, then a plan

The person tested absorbs it privately first, then works out with the counsellor how and to whom it should be passed on. This gives them time to settle their own feelings before facing anyone else's.

A written summary, shared quietly

Some families prefer a short written note relatives can read in their own time, followed by a call if questions come up. A note in Telugu often lands better with parents than an English report.

The elders told separately

In some households, older relatives are told in a slower, more private conversation than younger family members. There is no fixed order that suits everyone, and the right pace usually becomes obvious once you know the people involved.

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A practical way in

How to start the conversation at home

Lead with what it means, not the jargon

Start with "this means we should get your uncle checked" rather than reading out the gene name and classification first.

Say plainly what is not certain

Make clear that a fault raises risk rather than guaranteeing illness, before anyone starts assuming the worst.

Name who it actually affects

Be specific about which relatives the counsellor said should consider testing, rather than leaving the whole family unsure.

Offer the counsellor's number, not your own explanation

You do not have to answer every question yourself. Passing on a direct route to the counsellor takes the pressure off you.

Language that helps

Words worth having ready before the conversation

Family letter
A short written note, often prepared with the counsellor, that a relative can be given to explain the finding accurately.
First-degree relative
A parent, sibling or child. Usually the first group a counsellor will ask about and recommend testing for.
Disclosure
The act of telling a relative about a genetic finding that affects them. It is entirely the family's choice, not something anyone can be forced into.
Joint counselling session
An appointment where more than one family member meets the counsellor together, so everyone hears the same explanation at once.
Family tree (pedigree)
A drawn map of who in the family was diagnosed with what and at what age, used to work out who else should be considered for testing.
Confidentiality
Your own result is your information to share or not. Nobody, including a relative, can access it without your consent.

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Side by side

Sharing it well, and sharing it badly

Tends to work Tends to cause confusion
A written summary relatives can reread A single verbal retelling, passed on again
Naming exactly who should get tested Telling the whole family "everyone is at risk"
Offering the counsellor's contact number Trying to answer every medical question yourself
Saying plainly that risk is not certainty Letting fear fill in the gaps left unexplained

Being straight with you

What this page cannot tell you

It cannot tell you how your particular family will react, or which relative to worry about most. Families are different, and some conversations that sound difficult in advance go smoothly, while quieter ones turn out harder than expected.

It cannot write your family letter for you

A family letter needs your actual result and your actual family tree in it. A counsellor will help draft one specific to your situation rather than a generic template, and will usually go through the wording with you before it is sent to anyone.

Who this does not apply to

If your result was negative and does not point to anything relatives need to act on, there may be nothing urgent to disclose beyond simply letting people know the outcome. Not every result changes what the rest of the family needs to do, and a calm, brief update is often all that situation calls for.

If you are dreading a particular conversation, say so to the counsellor beforehand. They can help you plan exactly what to say and to whom.

Commonly believed

Four things families assume about sharing a result

"If I don't tell anyone, it stays private and nobody is affected."

Staying quiet is your right, but it also means relatives who could benefit from testing never get the chance to ask for it. It is a genuine trade-off, not a neutral choice.

"Younger family members do not need to know yet."

For adult-onset conditions, most counsellors agree that testing itself can wait, but knowing there is a family history worth asking about later usually should not be delayed indefinitely.

"One conversation should be enough to explain everything."

Most families need to revisit the topic more than once as questions surface later. Treating it as a single, one-time talk often leaves gaps.

"Telling relatives will only frighten them for nothing."

A clear, accurate explanation tends to reduce fear rather than cause it, because it replaces guessing with a specific next step relatives can actually take.

Questions we are asked

Common questions about sharing a report

Do I have to tell my relatives about my result?

No, it is your choice. A counsellor will explain who could benefit from knowing, but the decision to disclose stays with you.

Can the counsellor talk to my family directly?

Yes, with your consent. Many families arrange a joint session, or ask the counsellor to speak with a specific relative once the family agrees.

What if my family does not want to hear about it?

You cannot force the conversation. Leaving a written summary or the counsellor's contact details with them means they can come back to it when they are ready.

Should children be part of this conversation?

For most adult-onset conditions, detailed conversations usually wait until children are old enough to understand. A counsellor can advise on the right approach for your specific gene and family.

How do I explain a variant of uncertain significance to family?

Explain that the laboratory found a spelling difference it cannot yet classify, and that it should not change anyone's care for now. It is not a reason to test relatives.

Can I get a written summary to hand to relatives?

Yes, ask your counsellor for a family letter. It is written specifically to be shared and is usually easier to pass on than the full technical report.

What if relatives live in another city or state?

A written summary works well over distance, and many counsellors can also speak with a distant relative by phone once you have given consent.

Where do I start if I am unsure how to raise this?

Call the helpline and describe your family situation. Someone will help you plan the conversation or arrange a joint session with a counsellor.

Your Specialists

Meet CION's oncologists. Bring your family history or genetic report to them.

Our medical oncologists see people with a strong family history of cancer, arrange genetic counselling and testing where it fits, and plan the checks that follow.

Dr. Naresh Gundu
Medical Oncologist

Dr. Naresh Gundu

MBBS, DNB (Internal Medicine), DM (Medical Oncology)

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Dr. C. Raghavendra Reddy
Medical Oncologist

Dr. C. Raghavendra Reddy

MBBS(Gold Medal), DNB(General Medicine), DM(Medical Oncology)(Gold Medal)

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Dr. Bharati Devi Gorantla
Medical Oncologist

Dr. Bharati Devi Gorantla

MBBS, MD(General Medicine), DM(Medical Oncology)(Adyar,Chennai), ECMO, MRCP SCE(UK)

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Dr. Owais Mohammed
Medical Oncologist

Dr. Owais Mohammed

MBBS, MD (General Medicine), DrNB (Medical Oncology), ECMO, MRCP SCE (Medical Oncology) (UK)

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Dr. T. Raghavender Reddy
Medical Oncologist

Dr. T. Raghavender Reddy

MBBS, DM (Medical Oncology), MD (Radiation Oncology)

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Dr. N. Kiranmayee
Medical Oncologist

Dr. N. Kiranmayee

MBBS, DM (Medical Oncology), MD (Internal Medicine)

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Sources

  1. GeneReviews (NCBI) — Genetic Counseling
  2. Cancer Research UK — Talking to your family about inherited cancer risk
  3. NHS — Predictive genetic tests for cancer risk genes

This page is general information, not a prescription. Do not change or stop any treatment based on what you read here. If anything is worrying you, contact your own treating team — or call our helpline and we will help you reach the right specialist.

Talk to us

Not sure how to raise this with your family?

Tell us about your family and we will help you plan the conversation, or arrange a joint session with a counsellor. One helpline serves every CION centre.

Call 1800 202 8726

Speak to an oncologist

Where to find us

Our centres in and around Hyderabad

Addressed by landmark, because that is how this city navigates. One helpline books a consultation at any of these centres, and your team will tell you where counselling and testing take place.

CION Ameerpet

Beside Blue Fox Hotel, Satyam Theatre Road

Begumpet SR Nagar Punjagutta
CION Kukatpally

Opposite Big Bazaar, Mumbai Highway

KPHB JNTU Bharat Nagar
CION L.B. Nagar

Anu Arcade, next to L.B. Nagar Metro station

Vanasthalipuram Nagole Hayathnagar
CION Tolichowki

Inside Premier Hospital, Khader Bagh Road

Mehdipatnam Attapur Rethibowli
CION Masab Tank

Mahavir Hospital, AC Guards, Lakdikapul

Lakdikapul Khairatabad Basheer Bagh
CION Banjara Hills

Road No. 12

Jubilee Hills Madhapur Film Nagar
CION Kompally

Suchitra Circle, NH-44

Suchitra Circle Alwal Dundigal
CION Balanagar

Balanagar Main Road

Balanagar Fatehnagar Moosapet
CION Siddipet

Lohith Sai Hospital, Shivaji Nagar

Gajwel Husnabad Dubbaka
CION Sangareddy

X Roads, Pothreddipalle

Narayankhed Zaheerabad Patancheru
Explore more

Cancer Genetics Topics

Browse CION’s cancer genetics guide — family history and testing, reading a report, genes and syndromes, family planning, cost and support in Hyderabad. Tap any topic to read more.

This guide: Understanding Your Genetic Test Report

How to read a germline genetic test report The five classifications on a genetic test report 'Pathogenic': what this word on your report means 'Likely pathogenic': how sure is this result? 'Variant of uncertain significance' in a germline report Why a VUS should not change your treatment 'Benign' and 'likely benign': the two calm classifications Variant reclassification: when a genetic result changes years later What to do if you receive a genetic reclassification letter Keeping your genetic report findable for years to come Making sense of the c. and p. notation on your report What the gene name and transcript number on your report mean Heterozygous, homozygous and compound heterozygous, explained Biallelic findings: when both copies of a gene are affected A negative genetic result: what it does and does not rule out Uninformative negative: the genetic result nobody explains True negative or uninformative negative: which one is yours? Secondary and incidental findings: results you were not looking for When your cancer test finds a non-cancer condition When genetic testing shows an unexpected family relationship Low-level mosaic findings on a germline genetic report Clonal haematopoiesis picked up on a genetic test When your genetic report says no reportable variants When a genetic test fails or comes back inconclusive Why two labs can classify the same variant differently Looking up your own variant in ClinVar Should you search for your genetic variant online? Getting the raw data behind your genetic report Getting a genetic report read again, by someone new What a complete genetic test report looks like When a genetic report needs to be corrected Going through a genetic report as a family

Breast, ovarian & multi-organ genes

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