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Detects mutations and deletions in the beta-globin (HBB) gene, used to diagnose beta-thalassemia and other hemoglobinopathies.
10,710 THB
Detects mutations in the UGT1A1 gene, which cause Crigler-Najjar syndrome, a disorder that affects bilirubin metabolism.
11,875 THB
Detects mutations in the CSF3R gene, which are linked to various blood disorders, including chronic neutrophilic leukemia.
9,723 THB
Detects mutations in the HFE gene, which can cause hereditary hemochromatosis, leading to excessive iron absorption.
11,550 THB
Detects mutations in the IDH1 and IDH2 genes, commonly found in leukemia and brain tumors.
12,350 THB
Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting females.
15,390 THB