This is a laboratory developed test and has not been cleared or approved by NABL. The test is used for research purposes and should not be considered as investigational. The result of genotyping should be interpreted in the full context of the patient’s clinical history, including family history, ethnicities, lifestyle, co-morbidities, and other pre-existing conditions.
Limitation:
This test will not detect all the known variants that result in altered or inactive tested genes. The test does not account for all the individual variations in the individual tested, but it is limited to only well-known annotated variants based on evidence level at a point in time. Absence of a detectable gene mutation does not rule out the possibility that a patient has different phenotypes due to the presence of an undetected polymorphism. The variant annotation and corresponding interpretations are subjected to change over the time as and when more information is available from databases/literatures. Several variant types, including Triplet repeat expansions, translocations and large copy number events are currently not reliably detected by the test. It is recommended that genomic sequencing data is periodically reinterpreted, especially when new symptoms arise.
Disclaimer:
This report is not valid for any medico- legal purpose. Correlate with your physician to know more about the variant details. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Only a Physician, Geneticist, Genetic counselor, or any relevant health professional should advice the patient on further treatment information. The above variant annotation and their corresponding interpretations are based on the current information available in databases/literatures and are subjected to change over time.
The test involves the use of reporting software. This document contains private and confidential health information protected by state laws.