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Reports Within

Parameters

Reports Within:

Parameter Include:

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

The maximum days the report can be obtained for the Whole Exome Sequencing Test - Carrier (Single) is 21 days.

What are the prerequisites for the test Whole Exome Sequencing Test - Carrier (Single)

  • Must be at least 18 years old
  • Must provide a signed consent form
  • Must not have any significant medical conditions that would interfere with the test
  • Must not be pregnant or breastfeeding
  • Must not have had a bone marrow transplant in the past year

What are the measure values for the test Whole Exome Sequencing Test - Carrier (Single)

  • Test Name: Whole Exome Sequencing Test - Carrier (Single)
  • Measure Values:
    • Gene Mutation Analysis
    • Variant Interpretation
    • Carrier Status Determination
    • Report Generation

What does this test Whole Exome Sequencing Test - Carrier (Single) identify?

Whole Exome Sequencing Test - Carrier (Single)

This test is designed to identify carriers of genetic mutations within the exome, which is the portion of the genome that encodes for proteins. Carrier status refers to individuals who have one copy of a mutated gene but do not display symptoms of the associated genetic disorder. Carriers can pass the mutated gene on to their offspring, who may be affected by the disorder if they inherit two copies of the mutated gene.

The Whole Exome Sequencing Test - Carrier (Single) specifically looks for mutations in the exome that are associated with genetic disorders such as cystic fibrosis, sickle cell anemia, and Tay-Sachs disease. By identifying carriers of these mutations, individuals can make informed decisions about family planning and potential risks to their future children.

Why is this test Whole Exome Sequencing Test - Carrier (Single) taken?

Whole Exome Sequencing Test - Carrier (Single) is taken to identify whether an individual carries a genetic mutation that could be passed on to their offspring. This test analyzes the exons, or protein-coding regions, of all genes in an individual's genome to detect any potential carriers of genetic disorders. It is particularly useful for individuals who are planning to start a family and want to assess their risk of passing on inherited conditions to their children.

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