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26330 ClariTest Core NIPS

ClariTest Core NIPS
Test Code: CLARSO
Synonyms/Keywords

​​Trisomy 21 (Down Syndrome), Trisomy 18 (Edward syndrome), Trisomy 13 (Patau syndrome),

ClariTest Core Non-Invasive Prenatal Screen (NON-NY)
Useful For

​Prenatal screening test for Down syndrome, trisomy 18, trisomy 13 and sex chromosome abnormalities.

Specimen Requirements
Fasting RequiredSpecimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​No​Whole Blood​​Kit test with two Cell-Free DNA White Top plastic tubes​10 mL​7 mL
Collection Processing Instructions

​Collect blood according to the instructions provided in the kit.

Required fields to be filled out on the Req.: Patient demographic and insurance info, appropriate diagnosis codes, pregnancy type (singleton, twin), IVF pregnacy (Y/N): if yes, donor egg {self/non-self} and age of egg at retrieval, estimated due date, maternal weight.

Specimen Stability Information
Specimen TypeTemperatureTime
​Whole Blood​Ambient​7 days
Performing Laboratory Information
Performing LocationDay(s) Test PerformedAnalytical TimeMethodology/Instrumentation
GenPath BioReference Laboratories​​Sunday through Saturday​​5-7 days​Microarray quantitation with DANSR assay and FORTE algorithm            
Synonyms/Keywords

​​Trisomy 21 (Down Syndrome), Trisomy 18 (Edward syndrome), Trisomy 13 (Patau syndrome),

ClariTest Core Non-Invasive Prenatal Screen (NON-NY)
Ordering Applications
Ordering ApplicationDescription
CernerClariTest Core NIPS​
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Fasting RequiredSpecimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​No​Whole Blood​​Kit test with two Cell-Free DNA White Top plastic tubes​10 mL​7 mL
Collection Processing

​Collect blood according to the instructions provided in the kit.

Required fields to be filled out on the Req.: Patient demographic and insurance info, appropriate diagnosis codes, pregnancy type (singleton, twin), IVF pregnacy (Y/N): if yes, donor egg {self/non-self} and age of egg at retrieval, estimated due date, maternal weight.

Specimen Stability Information
Specimen TypeTemperatureTime
​Whole Blood​Ambient​7 days
Useful For

​Prenatal screening test for Down syndrome, trisomy 18, trisomy 13 and sex chromosome abnormalities.

For more information visit:
Performing Laboratory Information
Performing LocationDay(s) Test PerformedAnalytical TimeMethodology/Instrumentation
GenPath BioReference Laboratories​​Sunday through Saturday​​5-7 days​Microarray quantitation with DANSR assay and FORTE algorithm            
For billing questions, see Contacts
For most current information refer to the Marshfield Laboratory online reference manual.