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Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.

105,000 THB

Detects the Factor II (prothrombin) mutation, which increases the risk of blood clots.

3,750 THB

Detects known family-specific variants, used for diagnosing inherited genetic disorders.

6,520 THB

Detects FGFR1 gene rearrangements, often linked to cancers like myeloproliferative disorders.

118,680 THB

Detects mutations in the FGF23 gene, associated with phosphate regulation disorders.

13,300 THB

Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.

7,245 THB

Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.

7,245 THB

Detects filarial parasites in blood, used to diagnose filariasis.

1,148 THB

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