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This is a sendout test. Please note that turnaround time is defined as the anticipated time from set up day to results release.
S51162: Monogenic Diabetes (MODY) Eval [885] Print View
Result      

PRIMARY
1 Whole Blood EDTA 8 (6) mL   Refrigerated - 10 Day(s)/Room Temperature - 10 Day(s)  
ALTERNATE

Detects deletions in the HNF4A, GCK, HNF1A, HNF1B genes and mutations in the HNF4A, GCK, HNF1A, HNF1B, and IPF1

Higher blood volumes ensure adequate DNA quantity, which varies with
WBC, specimen condition, and need for confirmatory testing. Patients,
0-3 years have higher WBC, yielding more DNA per mL of blood.
Setup Schedule
Monday-Friday

Reported (Analytical Time)
14-30 days

CPT Codes
81405x2,81404x2,81479,81406x2

The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

Notes
Profile Includes: GCK (MODY2) DNA Sequencing and Deletion Test, HNF4A (MODY1) DNA Sequencing and Deletion Test, IPF1 (MODY4) DNA Sequencing Test, TCF1 (MODY3) DNA Sequencing and Deletion Test, TCF2 (MODY5) DNA Sequencing and Deletion Test. Specimen Requirements: Pediatric: 2 mL (1 mL minimum) Transport Temperature: Room temperature Methodology: Sanger Sequencing and Multiplex Ligation-dependent Probe Amplification (MLPA)






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