When analysis of a patient's genome identifies a variant, but it is unclear whether that variant is actually connected to a health condition, the finding is ...

VUS. 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 VUS to know whether it ...

3 thg 11, 2022 · Senior Geneticist, Jennifer Schleit describes why variants are classified as a VUS and what can be done to advance reclassification.

VUS là hệ thống Anh ngữ chuẩn quốc tế NEAS lớn nhất Việt Nam với gần 30 năm phát triển. Đến nay, hệ thống đã có 80+ cơ sở tại 22+ tỉnh thành.

These are called variants of uncertain significance, or VUS. In the cancer setting, they are also sometimes referred to as variants of unknown therapeutic ...

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

20 thg 11, 2021 · However, a large fraction of the variants identified in cancer predisposing genes (CPGs) are of uncertain significance (VUS), and cannot be used ...

31 thg 5, 2022 · Introduction. Variations in a genetic sequence are classified as variants of uncertain significance (VUS) when the association with disease risk ...

Depending on the gene or genes tested, a variable percentage of patients will receive a test report stating that a variant of unknown significance (VUS) has ...

The testing found one or more variants of unknown significance (VUS). There is not currently enough information available to know if the VUS identified is ...