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.
On this page
- Should you have genetic testing before planning a pregnancy after breast cancer?
- Women commonly offered genetic testing
- Options for couples with a known mutation, in general terms
- The vocabulary, in plain language
- Honest realities of genetic testing and pregnancy
- What happens in genetic counselling
- How preimplantation genetic testing works
- Sharing genetic results with relatives
- Accessing genetic testing and counselling in India
- Tips for making genetic decisions as a couple
- What people assume about genetic testing and pregnancy
- Common questions about genetic testing before pregnancy
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
Not sure whether this applies to you?
Ask an oncologistWords 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?
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.
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
Each child has a one in two chance.
Many carriers have children; options exist.
Men can carry and pass on mutations too.
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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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.
Sources
- National Cancer Institute — BRCA gene changes: cancer risk and genetic testing
- European Society of Human Reproduction and Embryology — Good practice recommendations on preimplantation genetic testing
- 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.