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Detects mutations associated with Hemoglobin Constant Spring, a variant of alpha-thalassemia.
3,750 THB
Detects the HbH (Hemoglobin H) disease-causing gene, an alpha-thalassemia variant.
3,750 THB
Comprehensive genetic panel for detecting mutations linked to hereditary hearing loss.
107,100 THB
Detects the INT22 inversion mutation in Hemophilia A patients.
5,865 THB
Comprehensive genetic test for mutations in BRCA1 and BRCA2, associated with hereditary breast and ovarian cancers.
184,800 THB
Identifies mutations in the GJB1 gene associated with hereditary hearing loss.
17,338 THB
Screens for carrier status of 62 genetic disorders including thalassemia, SMA, and FMR1.
35,416 THB
Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.
9,713 THB
Detects expansion mutations in the HTT gene, used to diagnose Huntington’s disease.
7,770 THB
Detects mutations in the immunoglobulin heavy chain variable region (IGHV), used in diagnosing chronic lymphocytic leukemia (CLL).
34,000 THB
Measures insulin antibodies, used to assess autoimmune reactions in diabetes.
26,100 THB