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What you should leave a genetic result appointment with | CION Cancer Clinics

You should leave a genetic result session with four things: the full report, a plain-language summary, a plan for your own care and a named person to call. If a fault was found, you also need a letter for your relatives. This page is a checklist for the last few minutes of the appointment, so nothing important goes home only in your memory. 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

What should you have in your hand when you walk out?

You should leave a genetic result session with the report itself, a plain-language summary, a clear plan for your own care and a name to call. If a fault was found, you should also have a letter for your relatives. If any of these is missing, ask for it before you stand up.

Why paper matters more than memory

Result sessions are emotional. Most people remember the headline and very little else. A week later, a brother asks which gene it was and nobody is sure. A written copy stops the details being lost or changed as the news passes around the family, often by WhatsApp.

Why a plan matters more than the result

A result on its own does nothing. What changes your life is what happens next: which scans, which referrals, which relatives should be tested. You should know what the next step is, who arranges it and roughly when it happens, even if the honest answer is that nothing changes.

It is reasonable to ask the counsellor to write the next steps down in front of you before you leave.

Your leaving checklist

Which documents and answers should you ask for?

Keep these together in one folder, with a photo of each on your phone.

The laboratory report

The full report, not just a verbal summary. It names the gene, the exact change found and how the laboratory classified it. Relatives will need these details for their own tests.

Check that it shows

  • Your name spelled correctly
  • The gene name and the exact variant
  • The classification, such as pathogenic or uncertain

A plain-language summary

A clinic letter that says in ordinary words what the result means for you. It should be something you could show a family doctor in your district who has never seen a genetic report before.

A family letter

If a fault was found, a short letter explaining it to relatives and how they can be tested for the same fault. You can hand it over or send a photo of it to relatives who live elsewhere.

A plan and a named contact

What happens next for your own care, who arranges it, and a named person or clinic to call with questions. Ask how you will be told if the laboratory ever changes its view of your result.

If the result is uncertain, the plan should say that it does not change your care on its own.

Not sure whether this applies to you?

Ask an oncologist

Before you stand up

What should you check in the last few minutes?

Say the result back in your own words

Tell the counsellor what you think the result means. If you have misunderstood anything, this is the moment it comes out. It is not a test of you. It is a check that they explained it well.

Ask what changes for you

Ask directly whether your treatment, your screening or your follow-up changes. Ask who will arrange any new scans or referrals, and whether you need to book them yourself.

Ask who else in the family is affected

Ask which relatives could be tested and in what order. Brothers, sisters and children usually come first. Ask whether the other side of the family matters too.

Confirm how you will be contacted

Check that the clinic has your correct phone number and a second contact. Results are sometimes reclassified years later, and the clinic can only reach you if the details are current.

On your report

What the words on your report mean

Pathogenic
The change is known to break the gene and raise cancer risk. This is what people mean by a gene fault.
Likely pathogenic
Strong evidence that the change is harmful. In practice it is usually managed in the same way as pathogenic.
Variant of uncertain significance
Often written as VUS. The laboratory found a change but does not yet know whether it matters. It should not guide your care on its own.
Benign or likely benign
A harmless difference. Many labs do not list these on the report at all.
No variant detected
No fault was found in the genes tested. It does not rule out every inherited cause.
Reclassification
When the laboratory changes its view of a variant as new evidence appears. It can move in either direction.

Leave a number, we will call you

One field. No form to fill in, and no charge for the call.

By result type

What should you leave with, depending on the result?

If the result is You should also leave with
A fault was found A family letter, and referrals for screening or specialist advice
No fault was found A note on whether your family history still calls for closer screening
An uncertain result A clear statement that it does not change care, and how updates will reach you
The test could not be completed A plan for a repeat sample, and who pays for it

Being straight with you

What this page cannot tell you

It cannot tell you what your own result means. What your specific variant means is a question for the counsellor who ordered the test. This page only helps you make sure you leave with everything you need to ask that question properly.

It cannot replace a missed session

Some laboratories send reports straight to patients, with no counsellor involved. If that happened to you, the checklist above will feel incomplete, because nobody was there to write the plan. Book a session with a genetic counsellor to go through it. Do not act on a report you have only read alone.

Who this does not apply to

If your test looked only at the tumour, it answers a different question about the cancer itself, not about your family. That kind of result is covered under targeted therapy. Most people reading this will never need a germline test at all.

If you left without something on this list, call the clinic and ask for it. It is a normal request.

Commonly believed

Four things people assume after a result session

"The doctor told me the result, so I do not need the paper."

Relatives cannot be tested for your exact fault without the written details. A verbal summary passed through the family loses the one piece of information the next laboratory needs.

"A negative result means our family is in the clear."

It means no fault was found in the genes tested. If the family history is strong, closer screening may still be advised. Your summary should say which applies to you.

"An uncertain result is half positive."

It is not a positive result, and it should not lead to extra surgery or change your treatment. Most uncertain results that are later reviewed turn out to be harmless.

"Once I leave, the clinic is done with me."

Genetic results can be reviewed as science moves on. Knowing how the clinic will reach you, and when to check back, is part of a finished appointment.

Questions we are asked

Common questions about the end of a result session

Can I ask for the full laboratory report?

Yes. It is your result and you are entitled to a copy. Ask for the full report, not just a summary page. Keep the original safe and share photos or copies with relatives who need it for their own testing.

What if I was too upset to take anything in?

That is very common. Ask for a written summary and a follow-up call or second session a few days later. Most counsellors expect this and would rather go through it twice than have you leave confused.

Should I record the session on my phone?

Ask first. Many clinics are happy for you to record so you can listen again or play it to a spouse. If recording is not allowed, bring someone to take notes while you listen.

Who should I show the report to next?

Your oncologist, if you are being treated, and your family doctor. If a fault was found, close relatives who may want testing. Share it with care, because once it is forwarded you cannot control where it goes.

Do I need a family letter if no fault was found?

Usually not in the same form, because there is no exact fault for relatives to be tested for. Your summary may still advise relatives about screening based on the family history. Ask the counsellor whether anything should be passed on.

What does it mean if my result could be reclassified?

Laboratories review variants as new evidence appears. An uncertain result may later be called harmless, or rarely harmful. Ask whether the laboratory or the clinic will contact you, and keep your phone number up to date with them.

Can I get the summary in Telugu?

Ask. Even if the formal report stays in English, many counsellors will explain the key points in Telugu and help you write them down. A summary your parents can read themselves is worth asking for.

Who do I call if a question comes up later?

The named contact on your summary, ideally the counsellor who gave the result. If you do not have one, call the CION helpline and someone will direct you to the right person.

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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Want a specific doctor for your case? Mention them when booking.

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Sources

  1. MedlinePlus Genetics — What do the results of genetic tests mean?
  2. National Cancer Institute — Genetic Testing for Inherited Cancer Susceptibility Syndromes
  3. NHS — Predictive genetic tests for cancer risk genes
  4. Cancer Research UK — Inherited cancer genes and increased cancer risk

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

Left your result session without a clear plan?

Tell us what your report says and what you were told. We will help you work out what is missing and arrange a session to go through it. 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: The Genetic Counselling Process

What does a genetic counsellor actually do? Genetic counsellor, clinical geneticist or oncologist: who does what Genetic counselling in India: training and certification How to find a genetic counsellor in India Do you need a referral for genetic counselling? Booking a genetic counselling appointment How long does a genetic counselling session take? What to bring to your first genetic counselling appointment Who should come with you to genetic counselling? Pre-test counselling: what is covered before you test Drawing the pedigree: your family tree on paper Reading your pedigree: what the symbols mean Verifying your family's cancer history with records Risk assessment: how your number is worked out How do you choose which genetic test to have? Informed consent before a genetic test What you are consenting to: storage, reuse and research Secondary findings: deciding whether you want them reported Giving the sample for a genetic test Which sample is more reliable for a genetic test? Can a genetic test be done from a stored tissue block? Genetic testing after a relative has died How long a genetic test result actually takes Why a genetic result takes weeks to come back Getting through the wait for a genetic result Post-test counselling: what the result session involves How genetic results are given: in person, by phone or in writing What you should leave a genetic result appointment with The family letter after a genetic result: what to do next Telegenetic counselling: genetic advice without the travel Genetic counselling in Telugu: asking in your own language Changing your mind about a genetic test Getting a second opinion on genetic advice After genetic counselling: what happens next

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