Comprehensive Bleeding Disorder Panel

Requisition Form: Requisition Form

ANO6, AP3B1, BLOC1S3, BLOCK1S6, DTNBP1, F10, F11, F13A1, F13B, F2, F5, F7, F8, F9, FERMT3, FGA, FGB, FGG, FLI1, GATA1, GFI1B, GGCX, GP1BA, GP1BB, GP6, GP9, HPS1, HPS3, HPS4, HPS5, HPS6, ITGA2B, ITGB3, LMAN1, LYST, MCFD2, NBEAL2, P2RY12, PLA2G4A, PRKACG, RASGRP2, RUNX1, SERPINA1, SERPINE1, SERPINF2, STIM1, TBXA2R, VIPAS39, VKORC1, VPS33B, VWF

This genetic panel is optimized for the detection of germline variants in 51 genes known to cause bleeding due to disorders of coagulation and/or platelet function.

comp_bleeding_disorder_td.pdf

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

Room Temperature

2-5 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)

Fetal: Call Laboratory; Parental/Patient: 2 mL

81238, 81404, 81407, 81408, 81479

Capture hybridization and Next Generation Sequencing (miSeq) with supplementary Sanger for quality and coverage

21 days

Testing is performed 2x per week

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