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Known Familial Variant Test Request Form 5424 Glen ridge Drive NE | Atlanta, GA 30342 USA | phone: 844.664.8378 | fax: 678.225.0212 | minilabs.compartment NameDOBMNG Variant Investigation Program
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How to fill out known familial variant test

01
Gather all the necessary information about your known familial variant.
02
Review the instructions provided by the testing laboratory or healthcare professional.
03
Complete the required paperwork, including consent forms or medical history questionnaires.
04
Provide a blood or saliva sample as instructed.
05
Ensure proper transportation and delivery of the sample to the testing facility.
06
Wait for the results to be processed and analyzed.
07
Consult with a genetic counselor or healthcare professional to interpret the results.
08
Follow any recommended actions or recommendations based on the test results.

Who needs known familial variant test?

01
Individuals with a family history of a known genetic variant or mutation.
02
People who have a high risk of inheriting a specific genetic condition.
03
Patients with a diagnosed genetic disorder who want to determine if their family members are at risk.
04
Couples planning to have children who want to assess the risk of passing on a specific genetic condition.
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A known familial variant test is a genetic test that is used to identify specific genetic mutations that have been previously identified in family members. It helps to assess the risk of hereditary conditions.
Individuals who have a family history of genetic disorders or those who have been advised by a healthcare provider to pursue genetic testing for inherited conditions are typically required to file a known familial variant test.
To fill out a known familial variant test, individuals should provide relevant personal and family medical history, submit required identification, and include any previous genetic testing results if available.
The purpose of the known familial variant test is to determine if an individual carries specific genetic variants that are linked to hereditary conditions, facilitating informed medical decisions and family planning.
The known familial variant test must report the identified genetic variants, their clinical significance, the familial relationship of the individuals tested, and any relevant recommendations for further action or monitoring.
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