Carrier Screening
Non-returnable
Rs.80,000.00 - Rs.151,600.00
Comprehensive screening panel of 332 autosomal and X-linked recessive disorders. Useful for future parents to detect possible single gene disorders like thalassemia, Fragile X, Spinal Muscular Atrophy and many other serious disorders.
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Product Details
- Comprehensive screening panel of 332 autosomal and X-linked recessive disorders
- Sequencing at ≥ 20x coverage
- CNV reporting for 34 genes
- Additional assays for SMN1, FMR1 & CYP21A2 included
- Sequencing at ≥ 20x coverage
- CNV reporting for 34 genes
- Additional assays for SMN1, FMR1 & CYP21A2 included
- Turnaround time of 15 business days
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