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MYH9 Sequence Analysis

Order Code: 5765

Test Information

Sequence analysis of the MYH9 gene detects germline variants associated with MYH9 related disorders (MYH9-RD) characterized by macrothrombocytopenia with or without extra hematologic manifestations.

Sample Requirements

Amniotic Fluid, Buccal Swabs, Cultured Amniocytes, CVS, DNA, EDTA Bone Marrow, EDTA Whole Blood

Shipping Information

Room Temperature

Requested Volume

3-5 mL EDTA Whole Blood or Bone Marrow (lavender top), 3-4 Buccal Swabs, 1 ug DNA at 50 ng/uL, 7-15 mL Amniotic Fluid, 5-10 mg CVS, 2-T25 flasks cultured amniocytes or CVS (2x10^6 minimum)

Minimum/Pediatric Volume

Fetal: Call Laboratory; Parental/Patient: 2 ml

CPT Codes

81479

Method

Capture hybridization and Next Generation sequencing (MiSeq) with supplementary Sanger for quality and coverage or PCR and Bi-directional DNA sequencing

Turnaround Time

14 days

New York State Approval

Approved

DEX Z-Code™

Yes, visit app.dexzcodes.com

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