HL7.GENETICS
Laboratory39 LOINC codes in this class
47999-8DNA region name [Identifier]L53035-2DNA marker assessed [Identifier]L48002-0Genomic source class [Type]L51958-7Transcript reference sequence [ID]L48003-8DNA sequence variation identifier [Identifier]L69548-6Genetic variant assessmentL53577-3Reason for studyL53037-8Genetic variation clinical significance [Imp]L53040-2Genetic variation's effect on drug metabolismL69549-4Genetic knowledge reference [Identifier]L48018-6Gene studied [ID]L51961-1Genetic variation's effect on drug efficacyL48004-6DNA change (c.HGVS)L51968-6Discrete variation analysis overall interpretationL48005-3Amino acid change (pHGVS)L53039-4Genetic disease analysis overall carrier interpretationL51969-4Genetic analysis reportL50398-7Narrative diagnostic report [Interpretation]L47998-0DNA sequence variation display name [Text] NarrativeL48006-1Amino acid change [Type]L48008-7Allele name [Identifier]L48013-7Genomic reference sequence [ID]L48019-4DNA change typeL51957-9Placer DNA analysis test identifier [Identifier]L51959-5Range(s) of DNA sequence examinedL51963-7Medication assessed [ID]L51964-5Drug efficacy analysis overall interpretationL51965-2Pharmacogenetic analysis report DocumentL51967-8Genetic disease assessed [ID]L51970-2Individual allele identifier [Identifier]L53034-5Allelic stateL53036-0Filler DNA analysis test identifier [Identifier]L53045-1Reference sequence alteration [Identifier]L53721-7Amino acid marker assessed [Identifier]L69545-2DNA region of interest start [Identifier]L69546-0DNA region of interest stop [Identifier]L69547-8Genomic ref allele [ID]L69550-2Genetic knowledge reference [Type]L69551-0Genomic alt allele [ID]L