Targeted Variant, Fetal
Order Name
Targeted Var Fetal
Test Number: 5194969
Revision Date 03/21/2023
Test Number: 5194969
Revision Date 03/21/2023
Test Name | Methodology | LOINC Code |
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Targeted Variant, Fetal
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Polymerase Chain Reaction |
SPECIMEN REQUIREMENTS | ||||
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Specimen | Specimen Volume (min) | Specimen Type | Specimen Container | Transport Environment |
Preferred | 4 mL (3 mL) | Amniotic Fluid | Sterile Screwtop Container | Room Temperature |
Alternate 1 | See Instructions | See Instructions | See Instructions | Room Temperature |
Instructions | Specimen Type: Amniotic fluid or chorionic villus sample (CVS) or cultured cells or cordblood. Direct amniotic fluid or CVS specimen may be submitted; additional culture fee may be applied. Specimen Volume: Amniotic fluid: 10 mL or CVS: 10 mg or amniotic fluid and CVS culture: one confluent T-25 flask or 4 mL cordblood. If amniotic fluid or CVS are cultured at another facility, please maintain back-up cultures. Mininum Volume: Amniotic fluid: 10 mL or CVS: 10 mg or amniotic fluid and CVS culture: one confluent T-25 flask or 3 mL cordblood Collection: Standard sterile techniques. Transfer aseptically to sterile tubes. Amniotic fluid: Discard first 2mL of fluid aspirated to avoid maternal cell contamination. Specimen Storage: Maintain specimen at room temperature. Do not freeze. Special Instructions: The specific gene and variant(s) to be analyzed must be indicated on the test requisition form. Failure to indicate the gene and variant will result in testing delays. Please include a copy of the previously tested family member's laboratory report for documentation. Labcorp clients with 8 digit client account numbers should call 800-345-4363 and Labcorp Genetics & Women's Health clients with 6 digit client /subclient account numbers should call 800-255-7357 to speak with a laboratory genetic coordinator before collecting specimens. In some circumstances, specimens from both parents and other family members may be required. All fetal specimens, including cordblood, must be accompanied by a maternal blood, PurFlock buccal swab kit or Oragene Dx 500 saliva kit for maternal cell contamination (MCC). A separate requisition should be submitted with the maternal specimen. |
GENERAL INFORMATION | |
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Expected TAT | 14 - 21 days In some cases, additional time may be required for confirmatory or reflex tests. |
Clinical Use | This test is used for prenatal diagnosis for pregnancies at risk for known variants in genes included in any Inheritest or GeneSeq®: Cardio panel. This test includes all genes included in any Inheritest or GeneSeq®: Cardio panel except SMN1 and FMR1. |
Performing Labcorp Test Code | 482534 |
Notes | Labcorp Test Code: 482534 |
Lab Section | Reference Lab |