MLchartDataset catalogue

variant of unknown significance

Term · Oncology and biomedicine · MLC-T-ONC-009171

  1. 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 unknown significance to know whether it increases a person’s risk of developing a disease, such as cancer. Also called unclassified variant, variant of uncertain significance, and VUS.

  2. 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.

Table 1. Record
IdentifierMLC-T-ONC-009171
FieldOncology and biomedicine
Synonymsunclassified variant; variant of uncertain significance; VUS
ReferencesNCI Dictionary of Cancer Terms; NCI Dictionary of Genetics Terms
Record as JSON
{
  "id": "MLC-T-ONC-009171",
  "term": "variant of unknown significance",
  "field": "Oncology and biomedicine",
  "definitions": [
    "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 unknown significance to know whether it increases a person’s risk of developing a disease, such as cancer. Also called unclassified variant, variant of uncertain significance, and VUS.",
    "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."
  ],
  "synonyms": [
    "unclassified variant",
    "variant of uncertain significance",
    "VUS"
  ],
  "references": [
    "NCI Dictionary of Cancer Terms",
    "NCI Dictionary of Genetics Terms"
  ],
  "url": "https://mlchart.com/terminology/oncology/variant-of-unknown-significance/"
}

Record 17,121 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.