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Screens for genetic variations associated with various health conditions, disease risks, and lifestyle factors using SNP array and polygenic risk scoring.
43,600 THB
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Detects the presence of the SRY gene, used in determining male sex development.
4,000 THB
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Detects specific mutations in genes related to various genetic disorders and cancers, using Sanger sequencing.
11,400 THB
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Detects mutations in the alpha-globin gene, used to diagnose alpha thalassemia.
4,375 THB
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Detects mutations in the beta-globin gene, used for diagnosing beta thalassemia.
7,015 THB
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Detects mutations in FGFR3 gene associated with thanatophoric dysplasia.
17,290 THB
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Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.
8,505 THB
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Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.
8,505 THB
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A non-invasive prenatal test using maternal blood to detect chromosomal abnormalities in the fetus.
39,600 THB
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Non-invasive prenatal test (NIPT) that screens for chromosomal abnormalities across all chromosomes.
42,000 THB
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