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What to do if you receive a genetic reclassification letter | CION Cancer Clinics

If a letter says your genetic result has been reclassified, do not act on it alone. First find which way the result moved, then book time with the counsellor or doctor who ordered the test. Most letters settle an uncertain result as harmless. An upgrade can mean new screening and testing for relatives. This page walks you through the first fortnight after the letter arrives. 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

A letter says my genetic result has changed. What do I do first?

Find out which way the result moved, then book a conversation with the counsellor or doctor who ordered the test. Do not start, stop or cancel anything on the letter alone. Most letters bring good news, because the most common change is an uncertain result being settled as harmless.

Three things to find on the letter

Look for the old classification, the new classification and the date of the change. Check that your name, date of birth and sample number match your original report. The letter may come by post, by email or as a message forwarded from the lab, and it is often written in technical English.

Why you should not act on it alone

A reclassification letter is written for a doctor to interpret. The same new classification can mean different things depending on your own history, your family tree and any treatment you are already having. What your specific variant means is a question for the counsellor who ordered the test.

Keep the letter with your original report. The two belong together from now on.

Reading the change

What is the letter most likely telling me?

Almost every reclassification letter falls into one of these four groups. Each one leads somewhere different.

Uncertain, now harmless

The most common letter. A variant of uncertain significance, or VUS, has been settled as benign or likely benign. Your care now follows your family history alone, and relatives need no test for it.

Uncertain, now a real fault

Less common. The variant is now pathogenic or likely pathogenic, meaning disease-causing. This letter needs a prompt appointment, because screening may change and blood relatives can be offered testing.

Bring to the appointment

  • The letter and your original report
  • A list of relatives on both sides
  • Any scans or treatment since the test

A fault, now downgraded

Rare. A variant once called pathogenic is now thought harmless or uncertain. Past decisions, and any relatives tested for it, need to be looked at again with your doctor. Do not undo anything on your own.

A correction, not a change

Some letters only update how the variant is written or which gene name is used. The meaning is the same. File it with the original so future doctors see the current wording.

Not sure whether this applies to you?

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In the first fortnight

What should I do, step by step?

Confirm the letter is yours

Match the name, date of birth, lab name and sample number against your original report. Mistakes are uncommon, but worth ruling out.

Contact whoever ordered the test

That is usually your oncologist or genetic counsellor. If they have moved on, the hospital that ordered the test can direct you to someone who can read it.

Book a counselling appointment

An upgrade needs a proper conversation, not a quick phone call. Ask for one in Telugu if that is easier for you and your family.

Wait before telling the whole family

Share it once you understand it. The counsellor can help you decide who needs to know first and can prepare a family letter.

Update your own records

Keep both documents together, and tell every doctor who treats you that the classification has changed.

On the letter

The words you will meet, in plain language

Reclassified
The lab has changed what it says your variant means. The variant in your DNA has not changed.
Previous classification
What your original report said. The letter should show this beside the new one so you can compare them.
Amended report
A reissued report carrying the new classification. It replaces the meaning of the old report, not the record of it.
Evidence summary
A short paragraph explaining why the lab changed its view, such as new family studies or data from other labs.
Ordering clinician
The doctor or counsellor who requested your test. Labs usually send updates to this person first.
Cascade testing
Offering blood relatives a test for one known family variant, one branch of the family at a time.

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Side by side

If the result went up, and if it went down

Moved up to pathogenic Moved down to benign
Book a counselling appointment promptly Discuss it at your next routine visit
Relatives can be offered a targeted test Relatives need no test for this variant
Your screening plan may be revised Screening follows your family history
Tell every doctor who treats you Still tell them, so old notes are not followed

Being straight with you

What this page cannot tell you

It cannot tell you what your letter means for you. The same change can matter a great deal to one person and very little to another, depending on their history and treatment. Only someone who has your report, your letter and your family tree in front of them can answer that properly.

It cannot say whether the change is final

Classifications can be reviewed again as evidence keeps growing. A second change is uncommon, but a reclassified result is still the lab's best current judgement, not a last word. Ask your counsellor how any future update would reach you.

Who this does not apply to

If you have not had a germline test, meaning a blood or saliva test for inherited faults, this page is not about you. Changes to tumour test results are a separate subject, covered on the targeted therapy pages. And if your letter only corrects wording, there is usually nothing to act on.

If the letter reached a relative instead of you, the steps are the same. Take it to the doctor who ordered the test.

Commonly believed

Four things people assume when the letter arrives

"A letter from the lab must mean bad news."

Most reclassification letters settle an uncertain result as harmless. Many people feel alarmed opening the envelope and relieved once someone explains it.

"The first report was a mistake, so I cannot trust any of it."

The reading of your DNA was almost certainly right. The knowledge used to interpret it has moved on. That is why labs review old results in the first place.

"If it has been upgraded, I should book surgery straight away."

An upgraded result opens a discussion. Screening, medicines and preventive surgery are options to weigh with your doctor over time. Nothing needs deciding the week the letter arrives.

"My relatives do not need to hear about a downgrade."

They do if they were tested for the variant or changed their screening because of it. A downgrade can lift worry and unnecessary tests from several people.

Questions we are asked

Common questions about reclassification letters

Why did the letter come to me and not my doctor?

Labs differ. Some write to the ordering doctor only, some to the patient as well, and some send a copy to both. If yours came to you directly, forward it to the doctor who ordered the test and ask for an appointment to go through it together.

The doctor who ordered my test has left. Who reads it now?

Contact the hospital or clinic where the test was ordered and ask to be seen by their oncology or genetics team. Any qualified genetic counsellor or clinical geneticist can read the letter alongside your original report. Bring both documents to that appointment.

My result was upgraded. Do my children need testing now?

Adult children can usually be offered a test for that exact variant. For faults that raise risk only in adult life, testing of young children normally waits until they can decide for themselves. Your counsellor will tell you which situation your family is in.

My result was downgraded after I had preventive surgery. What now?

This is rare and very hard to take in. Ask for a joint appointment with your surgeon and the doctor who ordered the test. They will look at whether your family history still supported the decision and what follow-up you need. Support is available for this situation.

Does a reclassification letter cost anything?

Receiving the letter does not commit you to any cost. A counselling appointment to discuss it, a review you request yourself, and any testing offered to relatives may each carry a fee. Ask about charges when you book so that nothing comes as a surprise.

Should I tell my insurer about the change?

India has no dedicated law on genetic discrimination in insurance, and disclosure rules depend on your policy wording. This is worth raising with your counsellor and reading your policy carefully. Do not guess at an answer from websites written for other countries.

Can the classification change again?

It can, though a second change is uncommon. Each classification is the best judgement on the evidence available at the time. Keep both reports safe and keep your contact details current with the lab and hospital, so any later update can reach you.

How do I explain the letter to my parents?

Start with what it means for them in one sentence, not the gene name. Ask the counsellor for a short family letter, in Telugu if that helps. Offer the counsellor's contact so they can ask their own questions rather than relying on your retelling.

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. MedlinePlus Genetics — What do the results of genetic tests mean?
  2. ACMG (Genetics in Medicine) — Standards and guidelines for the interpretation of sequence variants
  3. ClinVar — About ClinVar
  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

Holding a reclassification letter you do not understand?

Bring the letter and your original report, and a counsellor will explain what has changed and what, if anything, you or your relatives need to do. Counselling is available in Telugu. 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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