Home
Forms Library
VistaSeq - Sample Report - Variant of Uncertain Significance (PDF)

VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) 2025

VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) Preview on Page 1

Show details

4 out of 5

46 votes

The document is a sample report for the VistaSeq℠ Hereditary Cancer Panel, detailing genetic testing results for a female patient. It indicates the detection of a heterozygous variant of uncertain significance in the PMS2 gene, which is associated with Lynch syndrome and increased cancer risk. The report recommends genetic counseling to discuss the implications of these findings. It also outlines the methodology used for testing and provides information on additional genes included in the panel.

Here's how it works

01. Edit your form online

Type text, add images, blackout confidential details, add comments, highlights and more.

02. Sign it in a few clicks

Draw your signature, type it, upload its image, or use your mobile device as a signature pad.

03. Share your form with others

Send it via email, link, or fax. You can also download it, export it or print it out.

The easiest way to edit VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) in PDF format online

Ease of Setup

DocHub User Ratings on G2

Ease of Use

DocHub User Ratings on G2

Working on documents with our comprehensive and user-friendly PDF editor is simple. Follow the instructions below to fill out VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) online easily and quickly:

Sign in to your account. Sign up with your email and password or register a free account to test the service prior to choosing the subscription.
Upload a form. Drag and drop the file from your device or import it from other services, like Google Drive, OneDrive, Dropbox, or an external link.
Edit VistaSeq - Sample Report - Variant of Uncertain Significance (PDF). Effortlessly add and highlight text, insert images, checkmarks, and signs, drop new fillable areas, and rearrange or remove pages from your document.
Get the VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) completed. Download your modified document, export it to the cloud, print it from the editor, or share it with other participants via a Shareable link or as an email attachment.

Benefit from DocHub, the most straightforward editor to quickly manage your paperwork online!

be ready to get more

Complete this form in 5 minutes or less

Get form

Got questions?

We have answers to the most popular questions from our customers. If you can't find an answer to your question, please contact us.

What does VUS mean?

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.

What is variant of uncertain significance analysis?

Definition. When analysis of a patients genome identifies a variant, but it is unclear whether that variant is actually connected to a health condition, the finding is called a variant of uncertain significance (abbreviated VUS).

What is VUS in cancer?

Somatic cancer panel testing often detects variants in cancer cells that have unknown or unclear effects on the cancer cells. These are called variants of uncertain significance, or VUS.

Should I worry about VUS in genetic testing?

However, as part of genetic testing, other types of variants are often found, including those called variants of uncertain significances (VUS). Benign or Likely Benign These are harmless variants. They are not expected to impact a persons health.

What is VUS in oncology?

A change in a genes DNA sequence that has an unknown effect on a persons health. There is usually not enough information about a VUS to know whether it increases a persons risk of developing a disease, such as cancer.

Related forms

be ready to get more

Complete this form in 5 minutes or less

Get form

What does it mean if a result came back as a variant of uncertain clinical significance?

If the classification of the variant is as a VUS, it means that, at the time of interpretation, there was not sufficient evidence to determine if the variant is related to disease or not. It might be that the variant in question is rare, but has not been identified in affected individuals.

VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) 2025

Here's how it works

The easiest way to edit VistaSeq - Sample Report - Variant of Uncertain Significance (PDF) in PDF format online

Complete this form in 5 minutes or less

Got questions?

What does VUS mean?

What is variant of uncertain significance analysis?

What is VUS in cancer?

Should I worry about VUS in genetic testing?

What is VUS in oncology?

Complete this form in 5 minutes or less

People also ask

What does it mean if a result came back as a variant of uncertain clinical significance?

Related links

Try more PDF tools