Specialized Testing
Molecular Diagnostics
Genetic testing involves molecular analysis of human DNA, RNA, genes, and chromosomes to detect whether or not a person has an inherited trait or disorder, an acquired genetic alteration, a spontaneous genetic mutation, or is a carrier of a gene that could lead to a particular disorder or disease. Genetic Testing Payment Information Molecular Pre-Authorization Requisition FormMany insurances are requiring pre-authorizations for genetic and molecular testing. If noted above the patient’s insurance company is requiring the ordering physician to obtain a pre-authorization before additional testing can be performed. The Hyperlink below will provide a printer friendly alert values pages. Once open click the Printer Icon on the left side in the toolbar just above the form. |
The molecular diagnostic testing performed at RML uses a variety of methods including Polymerase Chain Reaction (PCR) and the Invader technology®. All molecular diagnostic testing will include a written pathology report. Result turnaround time will vary between 7-14 days.
Click here to learn more about our Cystic Fibrosis Carrier Screening.
Click on the Test Name below to view the Test Directory for more information and collection instructions.
Test Name: | Order Name: | Test Number: | Specimen: |
---|---|---|---|
EGFR Mutation Analysis (TK Domain) *NEW | EGFR MUTAT | 9103095 | Paraffin Block |
KRAS Mutation Analysis (K-ras) | KRAS MUTAT | 9100040 | Paraffin Block |
JAK 2 Mutation (V617F) Analysis | JAK2 MUTAT | 9100185 | EDTA WB |
Cystic Fibrosis 46 specific mutations | CYSTIC GEN | 1515700 | EDTA WB |
Factor 5 (V) Leiden Mutation Analysis | FACT 5 LEI | 9107735 | EDTA WB |
MTHFR, DNA Mutation Analysis (C665T & A1286C) (Methylenetetrahydrofolate Reductase) |
MTHFR | 1515625 | EDTA WB |
Factor 2 (II) Prothrombin Mutation 20210 Analysis | FAC II MUT | 1515300 | EDTA WB |
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