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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

Detects the presence of the SRY gene, used in determining male sex development.

4,000 THB

Detects mutations in the SURF1 gene, associated with Leigh syndrome.

18,620 THB

Detects specific mutations in genes related to various genetic disorders and cancers, using Sanger sequencing.

11,400 THB

Detects mutations in the alpha-globin gene, used to diagnose alpha thalassemia.

4,375 THB

Detects mutations in the beta-globin gene, used for diagnosing beta thalassemia.

7,015 THB

Detects mutations in FGFR3 gene associated with thanatophoric dysplasia.

17,290 THB

Detects MTHFR mutations, used to assess risk for thrombophilia.

3,250 THB

Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.

8,505 THB

Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.

8,505 THB

A non-invasive prenatal test using maternal blood to detect chromosomal abnormalities in the fetus.

39,600 THB

Non-invasive prenatal test (NIPT) that screens for chromosomal abnormalities across all chromosomes.

42,000 THB

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