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A second opinion on your genetic result in Hyderabad | CION Cancer Clinics

You can get a second opinion on an inherited gene result in Hyderabad, and it usually needs no new blood sample. A clinical geneticist or counsellor reviews your report, your family history and the current evidence about the variant. This page explains which results most deserve a second look, how the review works, and what it can and cannot change. 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

Can I get a second opinion on a genetic result in Hyderabad?

Yes. A clinical geneticist or genetic counsellor at another centre in Hyderabad can review your report, your family history and, where needed, the laboratory's raw data. Most second opinions need no new blood sample. They are a fresh reading of the evidence you already have.

Why a second reading can differ

A genetic report is an interpretation, not a simple yes or no. Laboratories weigh the evidence about each variant and place it in one of five groups, from harmless to disease-causing. Two careful laboratories can place the same variant in different groups, and evidence changes over time. A report from some years ago may read differently today.

When it is worth asking

Ask when a big decision rests on the result. That includes preventive surgery, a change in cancer treatment, testing children, or a choice about pregnancy. Ask too when the result does not fit the family story, such as a clear negative in a family with many young cancers. A second opinion is also sensible when nobody explained the report to you in the first place, which happens more often than it should.

Asking for a second opinion is normal practice. A good counsellor will not be offended and will help you gather what is needed.

Situations we see

Which results most often deserve a second look?

These are the situations where a fresh review most often changes the advice a family receives.

A VUS being treated as positive

A variant of uncertain significance means nobody yet knows whether it matters. If surgery or relatives' testing is being planned on the strength of one, a second look is urgent. Most uncertain variants that are later settled turn out to be harmless, which is why acting on one early can do real harm.

A negative that does not fit

A family with many young cancers and a clean result may have had the wrong person tested, or too narrow a test. A reviewer checks what was actually looked for.

Things a reviewer checks

  • Which genes were on the panel
  • Whether the affected relative was tested first
  • Whether large deletions were looked for

An old report

Variant classifications are updated as evidence grows. A result from several years ago may have been reclassified since, in either direction. Laboratories do not always write to patients when this happens, especially if the doctor who ordered the test has moved on. A review brings the old result up to date.

A report from a kit

Results from tests bought directly online, without a counsellor, often need confirming in a clinical laboratory before anyone acts on them. Some look only at a handful of common variants and miss the rest of the gene.

Not sure whether this applies to you?

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Step by step

How does a second opinion on a genetic report work?

Gather the paperwork

The full report, not a summary. Add the family history on both sides, pathology reports and any letters from the first counsellor.

The review appointment

A clinical geneticist or counsellor goes through the report and redraws the family tree. This can be in person or by video.

Checking the variant

The reviewer checks how the variant is classified in public databases and by other laboratories, and whether new evidence has appeared.

Contacting the laboratory

If there is doubt, the reviewer may ask the original laboratory to re-examine its classification or share its raw data.

A written opinion

You should leave with advice in writing: whether the result stands, what it means for you, and what the family should do next.

On your report

Second-opinion terms, in plain language

Reinterpretation
A fresh look at the same result using current evidence. No new sample is needed.
Reclassification
When a laboratory moves a variant to a different group, such as from uncertain to harmless.
VUS
Variant of uncertain significance. A spelling difference whose effect is not yet known. It should not guide treatment.
Pathogenic
Known to cause disease. Likely pathogenic means the evidence points strongly that way and is acted on the same way.
ClinVar
A free public database where laboratories share how they classify variants. It shows when laboratories disagree.
Raw data
The laboratory's underlying sequence files. Sometimes requested so another team can check a finding.

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Side by side

Reinterpreting the report, or testing again?

Reinterpretation A new test
No new sample needed A fresh blood or saliva sample
Right when the question is what a variant means Right when the first test was too narrow
Usually quicker and cheaper Costs and waiting time start again
Can be done from any city by video The sample can often be taken near home

Being straight with you

What a second opinion, and this page, cannot do

A second opinion cannot make an uncertain result certain. If the evidence about a variant is thin, a second expert may reach the same honest answer: nobody knows yet. That is still useful, because it stops a family acting on a guess. It also cannot undo decisions already made, though it can guide what happens next for you and your relatives.

What this page cannot tell you

It cannot tell you whether your own report is right. Please do not use it, or an online search, to judge your variant. What your specific variant means is a question for the counsellor who ordered the test, or for the qualified geneticist you see for the second opinion.

Who this does not suit

Most people with a clear result, explained properly by a counsellor, do not need a second opinion. It is not a way to get a different answer you would prefer. And somatic results from tumour testing, which guide cancer treatment, are reviewed by the oncology team rather than by a genetics clinic. If your question is about which cancer medicine suits a mutation found in the tumour, ask your oncologist about tumour testing instead.

Tumour mutation results belong to your oncologist. This page covers inherited results only.

Commonly believed

What people assume about a second genetic opinion

"A second opinion means taking the test again."

Usually it does not. Most second opinions are a review of the existing report and family history. A new test is needed only when the first one looked at too few genes or tested the wrong person.

"If two labs disagree, one of them made a mistake."

Often both followed the rules and weighed thin evidence differently. Disagreement is a signal that the variant is not yet well understood, and that caution is wise.

"My first doctor will be upset if I ask."

Second opinions are routine in genetics, where evidence moves quickly. Most counsellors welcome a colleague's view and will share records to help.

"I can check my variant online myself."

Public databases are written for specialists and are easy to misread. A variant name found online may not match your exact change. Bring the report to someone qualified instead.

Questions we are asked

Common questions about second opinions on genetic results

Who in Hyderabad can give a second opinion?

A clinical geneticist, or a genetic counsellor working with one, at a centre other than the one that gave the first advice. Your oncologist may suggest someone. Call the CION helpline if you are not sure where to go.

Do I need a new blood test?

Usually not. Most second opinions review the existing report. A new test is suggested only if the first was too narrow, tested the wrong relative or came from a kit that needs clinical confirmation before anyone acts on it.

What should I bring?

The complete report, every page of it, and any letters from the first counsellor. Add pathology reports for relatives with cancer and a written family history covering both sides, with rough ages at diagnosis.

Can I get my raw data from the laboratory?

Many laboratories will share it on request, sometimes only to a doctor. Ask the reviewer whether they actually need it. For most questions the report and the variant name are enough.

My result is a VUS and surgery has been suggested. What now?

Pause and seek a second opinion before deciding. A variant of uncertain significance should not by itself lead to preventive surgery. Decisions should rest on your family history and on any clearly harmful finding.

Can the second opinion be done online?

Often, yes. The review is mostly reading and talking, which suits a video call from a district. You will need to send clear copies of every page of the report beforehand.

What if the two opinions disagree?

Ask each to explain their reasons in writing. Often the disagreement is about how much weight thin evidence deserves. In that case the cautious course is usually to act on the family history rather than on the variant.

Will my relatives need to repeat anything?

Only if the result changes. If a variant is reclassified, relatives who were tested for it, or who were told they need not be, should hear about the change. The reviewer will explain who needs to be told.

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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Accreditation and empanelment

  • NABH
  • NABL
  • ISO 9001:2015
  • ArogyaSri empanelled
  • CGHS accepted
  • ECHS accepted
  • EHS accepted
  • Major cashless insurers

Paying for it

Insurance, schemes and payment

What you actually pay usually differs a great deal from the sticker figure.

AarogyasriEmpanelled. Bring the card and a referral where you have one.
CGHS / ECHS / EHSAccepted at CION centres for eligible treatment.
Cashless insuranceMost major insurers are empanelled. Pre-authorisation is handled by our desk.
Self-payItemised estimate given before treatment starts. No EMI scheme exists.

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

Sources

  1. Genetics in Medicine (ACMG and AMP) — Standards and guidelines for the interpretation of sequence variants
  2. National Center for Biotechnology Information — ClinVar
  3. ClinGen — Clinical Genome Resource
  4. National Cancer Institute — Genetic Testing for Inherited Cancer Susceptibility Syndromes

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

Is a big decision resting on your genetic report?

Tell us what the report says and what has been suggested. We will help you arrange a review by a qualified genetics team before you decide. One helpline serves every CION centre.

Call 1800 202 8726

Speak to an oncologist

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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.

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