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This test uses a reagent or kit labeled by the manufacturer as Research Use Only. 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.
81405-LDLR (low density lipoprotein receptor) (eg, familial hypercholesterolemia), duplication/deletion analysis
|Result ID||Test Result Name||Result LOINC Code|
LOINC and CPT codes are provided by the performing laboratory.