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This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
81381-HLA Class I typing, high resolution (ie, alleles or allele groups); 1 allele or allele group (eg, B*57:01P), each
|Test ID||Test Order Name||Order LOINC Code|
|HL58O||HLA-B*5801 Genotype, Allopurinol Hypersensitivity, Saliva||In Process|
|Result ID||Test Result Name||Result LOINC Code|
|35104||HLA-B 5801 Saliva Result||In Process|
|35105||HLA-B 5801 Saliva Interpretation||69965-2|
|35106||Reviewed by||No LOINC Needed|
LOINC and CPT codes are provided by the performing laboratory.