| parent | MOLPATH | LP7822-2 |
| child | HL7.GENETICS | LP70593-6 |
| child | HL7.CYTOGEN | LP111381-2 |
| child | Allelic frequency | LP212300-0 |
| child | Allelic phase | LP213621-8 |
| child | Allelic read depth | LP213622-6 |
| child | Associated phenotype | LP212301-8 |
| child | Basis for allelic phase | LP220487-5 |
| child | Cells.cytogenetic abnormality | LP410953-6 |
| child | Clinical cytogeneticist | LP62867-4 |
| child | Chromosome painting analysis | LP208607-4 |
| child | CIGAR | LP212299-4 |
| child | ClinVar version | LP232210-7 |
| child | Complex variant | LP212306-7 |
| child | COSMIC simple variant | LP213614-3 |
| child | COSMIC structural variant | LP213615-0 |
| child | COSMIC version | LP232209-9 |
| child | dbSNP | LP212297-8 |
| child | dbSNP version | LP213616-8 |
| child | Default genomic reference sequence coding system | LP212292-9 |
| child | Default transcript reference sequence coding system | LP217243-7 |
| child | Gene fusion transcript details | LP418370-5 |
| child | Gene studied with no variant found | LP411464-3 |
| child | Genetic diseases | LP62869-0 |
| child | Genetic form configuration controls | LP212393-5 |
| child | Genetic variant details | LP232001-0 |
| child | Variant exact start-end | LP212296-0 |
| child | Genomic coordinate system | LP343929-8 |
| child | Genomic structural variant copy number | LP213662-2 |
| child | Genomic structural variant name | LP213661-4 |
| child | Genotype display name | LP234803-7 |
| child | Haplotype name | LP234797-1 |
| child | HGVS version | LP212399-2 |
| child | Level of evidence | LP345149-1 |
| child | Nuclei scored | LP113318-2 |
| child | Origin of germline genetic variant | LP417220-3 |
| child | Precision of boundaries | LP212319-0 |
| child | Primer set | LP438600-1 |
| child | Range(s) of DNA sequences examined | LP212392-7 |
| child | Sample variant allelic frequency | LP343831-6 |
| child | Simple variant | LP212295-2 |
| child | Source of population allelic frequency data | LP343958-7 |
| child | Structural variant | LP212310-9 |
| child | Variant category | LP232211-5 |
| child | Variant coding system | LP213620-0 |
| child | Variant of unknown significance | LP411465-0 |
| child | Vendor FISH product name | LP199189-4 |
| child | Whole exome sequence analysis | LP248469-1 |
| child | Whole genome sequence analysis | LP248470-9 |
| child | Whole mRNA transcriptome sequence analysis | LP417648-5 |
| STATUS | NotStated |
| PartDisplayName | en-US | Genetics results |
LOINC Version: 2.80
FHIR