



Price-Rs. 2780 Rs 2499 /-
Thyrocare Triple Marker Test is a second-trimester prenatal screening done between 14 to 22 weeks of pregnancy to assess the risk of chromosomal abnormalities and neural tube defects in the developing baby. This test measures the levels of Alpha-fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), and Estriol (uE3) in the mother`s blood.
It helps screen for conditions such as Down Syndrome (Trisomy 21), Edward Syndrome (Trisomy 18), and Spina Bifida. The test is safe, non-invasive, and commonly recommended for women who missed the first-trimester double marker or need additional screening during pregnancy.
Book the Triple Marker Test online From Thyrocare & get Free home sample collection across India. All samples are tested in NABL/ISO-certified labs, ensuring fast, accurate, and pregnancy-safe reporting.

17 Crores+ Samples Processed

World Class Technology Labs

25+ Years of Trust & Experience

Free Home Collection
Price:
₹ 2,780.00 ₹ 2,499.00
100 Booked This Week
Sample Type: Blood
Fasting Not Required
List of Profiles Included:
- ALPHA FETO PROTEIN (AFP)
- BETA HCG
- UNCONJUGATED ESTRIOL (E3)
Booking Procedure:
- Technician from Thyrocare will be assigned for a free home sample collection after booking confirmation.
- Sample will be collected by our technician at your address at given slot.
- You will get a payment link in 2 hours. You can make the payment online or pay cash to the technician.
- Soft copy reports will be sent to your email address within 24 to 48 hours.
Frequently Asked Questions (FAQ's):
1. What is the Triple Marker Second Trimester test by Thyrocare?
The Triple Marker test in the second trimester is a prenatal screening conducted between 14–22 weeks of pregnancy. It measures levels of Alpha-Fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), and Unconjugated Estriol (uE3) to assess the risk of certain genetic conditions in the baby.
2. Why is the Triple Marker test important during pregnancy?
This test helps evaluate the risk of Down syndrome, Edwards syndrome, neural tube defects, and other chromosomal abnormalities, allowing doctors to recommend further diagnostic steps if needed.
3. Who should take this test?
It is recommended for all pregnant women, especially those above 35 years, with a family history of genetic disorders, previous pregnancy complications, or abnormal ultrasound findings.
4. When is the right time to take the Triple Marker test?
The ideal testing window is between 14 to 22 weeks of pregnancy, with 16–18 weeks being the most accurate period.
5. Is fasting required for the Triple Marker test?
No, fasting is not required. You can eat and drink normally before the test.
6. What type of sample is collected?
A blood sample is taken from the mother to measure the required markers.
7. How soon will I get the results from Thyrocare?
Reports are usually available within 3 to 5 working days, depending on the processing time and location.
8. Are the results diagnostic for birth defects?
No, the Triple Marker test is a screening tool, not a diagnostic test. Abnormal results indicate the need for further evaluation like amniocentesis or detailed ultrasound.
9. Is the Triple Marker test safe for mother and baby?
Yes, it is a completely safe and non-invasive blood test that poses no risk to the pregnancy.
10. Can I book the Triple Marker test at home?
Yes, Thyrocare offers free home sample collection, making it convenient for expecting mothers to get tested without visiting a lab.