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Carrier screening for common genetic conditions using next-generation sequencing and additional molecular methods.
35,840 THB
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Whole exome sequencing used to screen for hereditary cancer syndromes and cardiovascular diseases.
65,200 THB
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Whole genome sequencing to detect genetic mutations and variations across the entire genome.
103,500 THB
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Detects the XmnI polymorphism in the HBG2 gene, which can influence the severity of beta-thalassemia.
7,176 THB
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Determines zygosity for Hb CS-PS mutations using direct sequencing.
5,000 THB
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