Get Vistaseq - Sample Report - Variant Of Uncertain Significance (pdf)
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How to fill out the VistaSeq - Sample Report - Variant Of Uncertain Significance (PDF) online
The VistaSeq - Sample Report - Variant Of Uncertain Significance is a crucial document for understanding genetic testing results. This guide will provide you with clear, step-by-step instructions to assist you in completing the report accurately and efficiently online.
Follow the steps to fill out the form online.
- Click the ‘Get Form’ button to access the report and open it in your preferred PDF editor.
- Fill in the patient details section, including 'Date of Birth' and 'Patient ID'. Ensure that the date format is consistent and correct.
- Complete the specimen details including 'Specimen ID', 'Date Collected', 'Date Reported', and 'Specimen Type'. Use accurate dates and descriptions.
- In the client details section, provide the account number, name of the ordering physician, and address. This information should reflect the healthcare provider ordering the test.
- Review the results and interpretation section carefully. Make sure to note the gene and variant details, including 'Classification', 'Zygosity', and 'Amino Acid Change'.
- If applicable, consider filling in any recommendations or additional information regarding genetic counseling.
- Once all fields have been filled out, save your changes. You can then choose to download, print, or share the completed document as needed.
Start filling out your document online today for streamlined management of your genetic testing results.
A variation in a genetic sequence for which the association with disease risk is unclear. Also called unclassified variant, variant of uncertain significance, and variant of unknown significance.
Fill VistaSeq - Sample Report - Variant Of Uncertain Significance (PDF)
Variant and classify a variant as of uncertain significance when all other evidence suggests that it is benign. In result reports, variants in the following classifications are always reported, and are based on the following definitions and clinical recommendations. How to determine where a variant falls on the VUS spectrum. I have a VUS (Variant of Uncertain Significance). Targeted testing for these variant(s) is available for at-risk relatives. The clinical implications of the variant(s) of uncertain significance remain unclear. Some laboratories may report only pathogenic and likely pathogenic variants while others may report variants of uncertain significance as well. This is called a Variant of Uncertain Significance. A variant of unknown significance was detected in the BRCA1 gene, specifically p.A1142T. Variant classification categories include pathogenic, likely pathogenic, variant of uncertain significance.
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