Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Sep 2022. Module: SNOMED CT United Kingdom Edition module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 307561000237114 | Genetic variant of uncertain significance detected | en | Synonym | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| 307571000237116 | Genetic variant of uncertain significance detected (finding) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| 307581000237119 | Genetic variant of unknown significance detected | en | Synonym | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| 307591000237117 | Genetic VUS (variant of uncertain significance) detected | en | Synonym | Active | Only initial character case insensitive | SNOMED CT United Kingdom Edition module |
| 307601000237114 | Genetic variant of uncertain significance detection result positive | en | Synonym | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic variant of uncertain significance detected | Has interpretation | Detected | true | Inferred relationship | Existential restriction modifier | 1 | |
| Genetic variant of uncertain significance detected | Interprets | Molecular genetic test | true | Inferred relationship | Existential restriction modifier | 1 | |
| Genetic variant of uncertain significance detected | Is a | Evaluation finding | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR