Find and Order Laboratory Tests
Pharmacogenetics for Nevirapine (HLA-B*3505 allele):
4,500 THB
Detects the HLA-B*3505 allele to predict hypersensitivity reactions to Nevirapine, an antiretroviral drug.
EDTA whole blood >= 3 mL
Pharmacogenetic Panel
10840
Newborn Metabolic Disorders Screening:
10,290 THB
A comprehensive newborn metabolic disorder screening test using tandem mass spectrometry.
Dried Blood Spot, At least three drops of blood from heel (around 50 uL per drop) on Guthrie card.
Newborn Screening Panel
10809
Autism Genetics Tier 2 (Genome star):
123,900 THB
Comprehensive genetic analysis for autism-related gene variants.
EDTA blood 6 ml 1 tube
Genetic Testing
10825
Vista-Carrier Screening Target Panel PLUS:
34,000 THB
This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
EDTA Blood 5 ml.
None
10810
VISTA Carrier Screening Mini Panel PLUS:
35,840 THB
Carrier screening for common genetic conditions using next-generation sequencing and additional molecular methods.
EDTA Blood 5 ml or Saliva
Genetic Testing
10811
Panorama Extended Panel:
37,600 THB
A comprehensive NIPT panel that includes additional microdeletion syndromes.
2 tubes of 10 mL each of maternal blood(Special kit)
Prenatal Panel
10812
Panorama NIPT:
33,600 THB
A non-invasive prenatal test to detect common aneuploidies such as trisomy 21, 18, and 13.
2 tubes of 10 mL each of maternal blood
Prenatal Panel
10813
QF-PCR:
6,900 THB
This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
1.Aminiotic fluid 3 ml (minimum 1 ml) Or 2.Um- bilical cord blood in tube EDTA(PCR)
None
10814
Array CGH Optima:
33,600 THB
Detects chromosomal abnormalities through array CGH, useful for prenatal and postnatal diagnosis.
Amniotic fluid 15-20 ml 1. (Amniotic fluid) 15-20 ml 2. (umbilical cord blood) 1-5 ml 3. (Product of conception)
Genetic Testing
10815
QF-PCR & Karyotype:
12,075 THB
A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.
1. amniotic fluid 20 ml or 2. EDTA cord blood 1 ml + Heparine cord blood 3-5 ml 3. EDTA blood 1 ml + Heparin blood 3-5 ml
Prenatal Panel
10816
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