A means to bundle several observations such as one would find in a genetics test panel.

This is actually LOINC code 79742-3. And the IG will be updated

Predicted phenotype for drug efficacy through transport mechanism. A single marker interpretation value known to increase or decrease the drug's performance.

Finding of whether a particular somatic genotype/haplotype/variation or combination-thereof predicts a particular outcome for the specified cancer - either on its own or in conjunction with one or more interventions.

The non-medication therapy (procedure) associated with this implication.

Given as a number between 0 and 100. Mean mapped read depth. Obtained by counting total number of mapped reads and divided by the number of bases in the region sequence.

Annotated changes to sequence features caused by this variant. Terms are from the sequence ontology under SO:0001537.

The genomic coordinates of the exact genomic range in which the variant resides.

The genomic coordinates of the inner genomic range in which the variant might reside.

The genomic coordinates of the outer genomic range in which the variant might reside.

A quality inhering in a variant by virtue of its origin. The terms are in the sequence ontology under SO:0001762.

An observation linking a genomic finding with a knowledge base, providing context that may aid in diagnosing a patient with a particular phenotype or condition.

An observation linking a genomic finding with a knowledge base, providing potential evidence of an interaction with a specified medication or non-medicinal therapy.