LAB13271 - CHS Lab Directory

Result Test Name PANEL SUMMARY QUEST

Laboratory QUEST LAB

Result Test Code 12386008418

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC -

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name INTERP

Laboratory QUEST LAB

Result Test Code 123012583

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 38404-0

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name INTERPRETATION

Laboratory QUEST LAB

Result Test Code 3644

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC -

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name SMA 2+0 RISK VARIANT

Laboratory QUEST LAB

Result Test Code 12386026711

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC -

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name CF RESULT

Laboratory QUEST LAB

Result Test Code 123012582

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 21654-9

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name METHOD

Laboratory QUEST LAB

Result Test Code 123012585

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 49549-9

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name SMN1

Laboratory QUEST LAB

Result Test Code 123012313

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 35462-1

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name MUTATIONS/POLYMORPHISMS

Laboratory QUEST LAB

Result Test Code 123012584

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 21656-4

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name ETHNICITY

Laboratory QUEST LAB

Result Test Code 123012581

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 32624-9

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name SMN2

Laboratory QUEST LAB

Result Test Code 123012314

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 54449-4

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name TECHNICAL RESULTS

Laboratory QUEST LAB

Result Test Code 3645

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC -

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name REVIEWER

Laboratory QUEST LAB

Result Test Code 123012586

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC 69047-9

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -

Result Test Name FRAGILE X PCR

Laboratory QUEST LAB

Result Test Code 12301086006221

Laboratory Test Name Prenatal Carrier Screen

Reportable Test Name -

Result LOINC -

Collection Container Purple Top - EDTA

Units -

Collection Requirements Preferred Specimen(s) 4 mL whole blood collected in an EDTA (lavender-top) Minimum Volume 3 mL Collection Instructions Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Transport Container Original collection tube Transport Temperature Room temperature

Container Temp Room Temperature (1)

Container Volume 4.000

Test Info This Quest Test Code 90949 Clinical Significance Prenatal Carrier Screen (CF Fragile X SMA) - This panel identifies individuals at risk of having offspring with Cystic Fibrosis (the most common life-limiting autosomal recessive disease) Fragile X syndrome (the most common cause of inherited intellectual disability) and Spinal Muscular Atrophy (the second most common lethal autosomal recessive disease).

Shipping Instructions -