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Fertility and menopause

Genetic testing before planning a pregnancy

Genetic results such as BRCA can shape pregnancy timing, ovarian surgery decisions and choices for future children. Some couples use IVF with embryo testing, while many conceive naturally. Genetic counselling helps. This page explains testing, reproductive options and sharing results.

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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

Should you have genetic testing before planning a pregnancy after breast cancer?

Many women diagnosed with breast cancer at a young age, or with a strong family history, triple negative cancer, or certain other features, are offered genetic testing for inherited gene changes such as BRCA1, BRCA2, PALB2 and others. If you are planning a pregnancy, knowing your genetic results can be valuable for several reasons. First, a mutation in a gene such as BRCA1 or BRCA2 can affect decisions about timing, because women with these mutations are often advised to consider removing their ovaries and fallopian tubes once their family is complete, to lower ovarian cancer risk. Second, each child of a parent with such a mutation has a one in two chance of inheriting it. Some couples choose preimplantation genetic testing, known as PGT-M, during IVF to select embryos without the family mutation, where available and legally permitted. Others choose natural conception and may consider testing during pregnancy or testing the child later in adulthood. Many choose not to test embryos at all. Third, results may matter for your partner and relatives, and some couples also consider testing the partner. Genetic counselling before and after testing is essential, because results can raise complex medical, emotional, ethical and financial questions, and a trained counsellor can help you understand all options without pressure.

Testing is a personal choice

No one should feel pressured to test or to use embryo testing.

Counselling comes first

A genetic counsellor explains what results mean before you decide.

Relatives may benefit

Your results can help family members make informed choices.

This page gives general information only. A genetic counsellor can advise on your situation.

Who is offered testing

Women commonly offered genetic testing

Criteria vary between centres and guidelines.

Young age at diagnosis

Especially under forty-five or fifty.

Triple negative cancer

More often linked to BRCA1 mutations.

Family history

Relatives with breast, ovarian, prostate or pancreatic cancer.

Both sides of the family count.

Other features

Cancer in both breasts, or male relatives with breast cancer.

Genes commonly tested

  • BRCA1 and BRCA2
  • PALB2
  • TP53 and others

Reproductive options

Options for couples with a known mutation, in general terms

Option What it involves
Natural conception without testing Many couples choose this, accepting the chance of passing on the mutation
IVF with PGT-M Embryos tested for the family mutation before transfer
Donor eggs or sperm Using gametes from a donor without the mutation
Testing the child in adulthood Leaving the choice to the child when they are old enough
Adoption An alternative path to parenthood

Not sure whether this applies to you?

Ask an oncologist

Words you will hear

The vocabulary, in plain language

BRCA1 and BRCA2
Genes that, when altered, raise breast and ovarian cancer risk.
PGT-M
Testing embryos for a specific inherited gene change during IVF.
Genetic counselling
Discussion with a trained professional about genetic testing and results.
Carrier
A person who has an inherited gene change.
Variant of uncertain significance
A gene change whose effect on risk is not yet known.
Risk-reducing surgery
Surgery to lower future cancer risk, such as removing ovaries.

Being straight with you

Honest realities of genetic testing and pregnancy

Genetic information can be empowering, but it can also be complex.

Results are not always clear

Some tests find variants of uncertain significance, which do not guide decisions.

Embryo testing has limits

PGT-M requires IVF, adds cost, and may reduce the number of embryos available.

Access and regulation vary

Availability of embryo testing in India depends on clinics and regulations.

Ethical questions

Couples may have different views about testing embryos. Counselling helps.

What this page cannot tell you

It cannot tell you which option is right. A genetic counsellor can help you decide.

Genetic counselling

What happens in genetic counselling

Genetic counselling helps you understand testing and results before making decisions.

Family history

The counsellor draws a family tree, including cancers on both sides of the family.

Explaining tests

You learn which genes are tested, possible results and what they could mean.

Discussing implications

Implications for your cancer care, pregnancy plans, children and relatives are discussed.

Consent

Testing is only done with your informed consent.

After results

A follow-up appointment explains results and next steps.

Talk to our team

Have a question about your situation?

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Embryo testing

How preimplantation genetic testing works

PGT-M allows couples to choose embryos without a known family mutation.

IVF cycle

Eggs are collected and fertilised to create embryos, using protocols suitable after breast cancer.

Embryo biopsy

A few cells are taken from each embryo at an early stage and tested.

Selecting embryos

Embryos without the mutation are chosen for transfer or freezing.

Confirmation

Testing during pregnancy may be offered to confirm results.

Costs and availability

PGT-M adds cost and is available at selected centres.

Family

Sharing genetic results with relatives

Your results may help relatives understand their own risk.

Who may benefit

Parents, siblings, children and other close relatives may be offered testing.

How to share

Genetic counsellors can provide letters to help explain results to family members.

Respecting choices

Some relatives may not want to know. Their choice should be respected.

In India

Accessing genetic testing and counselling in India

Genetic testing for inherited breast cancer risk has become more widely available in India, but access and costs still vary.

Where testing is offered

Many large cancer centres and teaching hospitals offer genetic counselling and testing, often through partnerships with accredited laboratories. Your oncologist can refer you.

Choosing a laboratory

Ask whether the laboratory is accredited, which genes are included in the panel, and how results will be explained. Direct-to-consumer tests may not be suitable for medical decisions.

Costs and coverage

Costs vary with the number of genes tested. Insurance coverage is limited, but some hospitals, research programmes and charities offer support.

Testing relatives

Once a mutation is found in the family, testing relatives for that specific change is usually simpler and less costly.

Embryo testing access

PGT-M is available at selected fertility centres and must follow national regulations on assisted reproduction. Ask the clinic about experience, success rates and consent requirements.

Privacy

Ask how your genetic information will be stored and who can access it.

Making decisions

Tips for making genetic decisions as a couple

Genetic results can raise deep questions about family and the future.

Take your time

Unless timing is urgent, allow yourselves weeks to think and talk.

Consider each other's values

Religious, cultural and personal beliefs can shape views on embryo testing, donor use or testing children. Respecting these differences helps couples reach choices both partners can live with.

Think about extended family

Decide together how and when to share results with parents, siblings and in-laws, as genetic news can affect the wider family.

Seek support if you disagree

If you and your partner see things differently, a genetic counsellor or psychologist can guide calm conversations without taking sides, helping each person feel heard.

Remember timing

If your oncologist has advised a particular window for pregnancy, factor this into how long you take to decide about testing.

Look after your wellbeing

Genetic decisions can feel heavy. Rest, exercise and time with loved ones help you think clearly.

Use trusted sources

Rely on your counsellor and reputable medical sources rather than forums.

Write down questions

Bring them to your genetic counsellor so nothing is missed.

Commonly believed

What people assume about genetic testing and pregnancy

If I carry BRCA, my children will definitely inherit it.

Each child has a one in two chance.

Carrying BRCA means I should not have children.

Many carriers have children; options exist.

Genetic testing is only for women.

Men can carry and pass on mutations too.

Embryo testing is compulsory for carriers.

It is always a personal choice.

Questions we are asked

Common questions about genetic testing before pregnancy

Should I get tested before trying to conceive?

If you meet testing criteria, results can help planning. Ask your team.

Is PGT-M available in India?

It is offered at selected centres, subject to regulations.

Should my partner be tested?

Sometimes, depending on family history. Ask a genetic counsellor.

How long do results take?

Usually a few weeks.

Does a BRCA mutation affect pregnancy safety?

Studies suggest pregnancy is generally safe for carriers.

When should ovaries be removed?

Timing depends on the gene and family plans; discuss with your team.

Can my children be tested?

Testing is usually offered in adulthood.

Who can help me decide?

A genetic counsellor and your oncologist.

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Talk to our team

Speak to a breast cancer specialist

Call the helpline or leave your details, and someone will help you arrange a consultation at the CION centre nearest you. One helpline serves every CION centre.

Call 1800 202 8726 Helpline open 24/7

Request a call back

Share your number and a specialist's team will call you.

Free call back. Your details stay private.

Sources

  1. National Cancer Institute — BRCA gene changes: cancer risk and genetic testing
  2. European Society of Human Reproduction and Embryology — Good practice recommendations on preimplantation genetic testing
  3. National Comprehensive Cancer Network — Genetic/familial high-risk assessment: breast, ovarian and pancreatic

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.

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