Why genetics matters before pregnancy
Carrier & compatibility screening
Know if both partners carry the same recessive variant.

Inherited Risk Context
Understand predispositions relevant to planning & prenatal care
Actionable next steps
Clear, counsellor-guided options to discuss with your Doctor
Medication & Fertility
Pharmacogenomic signals to discuss with your clinicians
What you get with myCodexa
Whole Genome Sequencing (WGS)
Clinical grade analysis at our CAP & NABL accredited Lab (not outsourced)
Inherited Risk Context
Side by Side interpretation for shared risk.
1:1 counselling
Results explained with practical next steps.
Data Privacy
Secure, consent based access; storage in India.
Fast Turnaround
Reports typically in 14 business days,
Concierge collection
Home/office phlebotomy collection as per your convenience
How it Works




FAQs
It’s a simple blood-based test that studies both partners’ genes to check if you carry variants that could affect your future child’s health. It helps you make informed reproductive choices before pregnancy.
myCodexa fully decodes your DNA and gives you a personalized report with a genetic expert who helps you and your doctor understand it and plan next steps. They also keep your report updated for three years.
Because it’s easier and safer to understand your genetic compatibility before conception. Knowing shared carrier risks early gives you time to discuss preventive or IVF options with your doctor.
Usually about 14 business days after your sample is received at our CAP & NABL-accredited genomics lab.
We'll arrange a blood draw at your home or a clinic. Before testing, a genetic counselor will explain the process. Your DNA will be thoroughly analyzed in a certified lab. You'll receive a personalized report, and a counselor will help you understand the results. We'll also provide guidance for your doctor, including information on medication interactions. Your report will be updated for three years as research advances, and we offer ongoing support via email.
Never without your consent. All data is stored securely in India under strict privacy and access-control policies. Only you and your designated counsellor can view your results.
Yes. Testing both partners helps identify shared carrier risks that single-person screening might miss, giving you the clearest picture for family planning.
For any questions or clarifications, please feel free to contact us at
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