81261-0
LOINC Code
| LOINC code | 81261-0 | |
|---|---|---|
| name | ||
| description | This term is used to report the formal name of a complex variant, including the reference sequence and details about the variation. For example, NM_000106.5(CYP2D6):c.[886C>T;457G>C] - Haplotype represents a CYP2D6 gene variant with haplotype nucleotide changes c.886C>T and c.457G>C and the NCBI reference sequence NM_000106.5. [http://www.ncbi.nlm.nih.gov/clinvar/variation/16895/] | |
| status | TRIAL | |
Fully-Specified Name | ||
| component | Complex variant name | |
| property | Find = Finding | |
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | |
| system | ^Patient | |
| scale | Nom = Nominal: Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody. | |
| method | ||
Additional Names | ||
| short name | Comp var; Comp var name; Compx; Finding; Findings; Molecular pathology; MOLPATH; Nominal; Point in time; Random | |
Basic Attributes | ||
| class | MOLPATH | |
| type | 1 Laboratory | |
| order vs. observation | Comp var name | |
History/Usage | ||
| first released | ||
| last updated | 2.58 | |
| last change type | MIN - change to field other than name | |
Related Names | ||
Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.
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