Test Code: FCGT06

Genes: HBB, HBA1, HBA2, SMN1, FMR1 (5 genes)

Sample Type: Lavender-top (EDTA) tube, 30-mL amniotic fluid in sterile falcon tubes, or two confluent T-25 flasks for fetal testing.

Method: MLPA, and Next Generation Sequencing

Turnaround Time: 10 days for Blood; Amniotic Fluid/CVS 14-20 days

Courier: Ship overnight at room temperature to receive next day. Maintain specimen at room temperature.

Price: 1100

Description:
Reproductive Carrier Screening helps identify whether someone carries certain inherited conditions that could affect future children. This panel looks at four important disorders: Alpha thalassemia, Beta thalassemia, Spinal muscular atrophy (SMA), and Fragile X syndrome (FXS). Identifying carrier status provides critical information for individuals and couples planning a family, helping to reduce the risk of passing on severe genetic conditions. It is especially useful for gamete donors, as it ensures donated eggs or sperm are screened for major genetic risks. By providing this information, the test supports safer family planning and healthier outcomes for future generations.