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Reports Within:

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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

Maximum Turnaround Time for Sanger Sequencing (SS) Variant Confirmation, Single Test:

The report for the Sanger Sequencing (SS) Variant Confirmation, Single Test can be obtained within 10 business days from the date of sample collection.

What are the prerequisites for the test Sanger Sequencing (SS) Variant Confirmation, Single Test

  • Specimen: DNA extracted from blood or bone marrow
  • Minimum Volume: 5 μL
  • Minimum Concentration: 20 ng/μL
  • Preferred Container: 1.5 mL microcentrifuge tube
  • Transport Temperature: Room temperature
  • Specimen Stability: 3 days at room temperature, 7 days refrigerated

What are the measure values for the test Sanger Sequencing (SS) Variant Confirmation, Single Test

  • Test Name: Sanger Sequencing (SS) Variant Confirmation, Single Test
  • Method: Sanger Sequencing
  • Sample Type: Blood, saliva, tissue
  • Turnaround Time: 7-10 days
  • Cost: $150-$300

What does this test Sanger Sequencing (SS) Variant Confirmation, Single Test identify?

Sanger Sequencing (SS) Variant Confirmation, Single Test

This test is used to identify and confirm variants in DNA sequences through Sanger sequencing. Sanger sequencing is a method of DNA sequencing that determines the order of nucleotides in a DNA molecule. This test can be used to identify single nucleotide polymorphisms (SNPs), insertions, deletions, and other genetic variations.

Why is this test Sanger Sequencing (SS) Variant Confirmation, Single Test taken?

Sanger Sequencing (SS) Variant Confirmation, Single Test is taken to confirm the presence of a specific genetic variant in an individual's DNA. This test is typically ordered after initial genetic testing has identified a potential variant of interest, and is used to validate and confirm the presence of this variant.

Sanger Sequencing is a widely-used method for DNA sequencing that allows for the determination of the exact sequence of nucleotides in a specific region of DNA. This technique is highly accurate and is often used in research and clinical settings for variant confirmation.

By confirming the presence of a specific genetic variant through Sanger Sequencing, healthcare providers can make more informed decisions regarding patient care, treatment options, and genetic counseling. This information can be crucial for individuals with genetic conditions or at risk for inherited diseases.

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