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  • Vistaseq - Sample Report - Variant Of Uncertain Significance (pdf)

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Vistas Hereditary Cancer Panel SAMPLE REPORT, VISTAS Patient Details 10 15/1978 DOB: Age y/m d): 036 08/06 Gender: F Patient ID: SAMPLE Specimen Details Specimen ID: Date Collected: Date Reported:.

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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.

A variation in a genetic sequence for which the association with disease risk is unclear. Also called unclassified variant, variant of uncertain significance, and VUS.

(VAYR-ee-unt … un-SER-tin sig-NIH-fih-kunts) A change in a gene's DNA sequence that has an unknown effect on a person's health. There is usually not enough information about a variant of uncertain significance to know whether it increases a person's risk of developing a disease, such as cancer.

The VUS rate is calculated as the total number of clinical myRiskâ„¢ reports with one or more VUS and no co-occurring pathogenic variants (PVs) as a function of the total number of clinical myRiskâ„¢ reports.

The testing for you/your family member found one or more variants of unknown significance (VUS) in a gene(s) that causes epilepsy. A VUS is a gene change, but there is not enough information available about this change to know if it causes epilepsy or not. Genes are instructions for how our bodies work and develop.

One of the five variant classification categories recommended by the American College of Genetics and Genomics (ACMG)1, a VUS classification means that there is insufficient or conflicting evidence regarding a molecular alteration's role in disease.

Variations in a genetic sequence are classified as variants of uncertain significance (VUS) when the association with disease risk and the significance to function are unclear. These VUS are usually missense, silent, intronic variants or in-frame deletions and insertions.

Lynch syndrome, often called hereditary nonpolyposis colorectal cancer (HNPCC), is an inherited disorder that increases the risk of many types of cancer, particularly cancers of the colon (large intestine) and rectum, which are collectively referred to as colorectal cancer.

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Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232