Also Known as
ANO6, AP31B, BLOC1S3, BLOC1S6, DTNBP1, FERMT3, FLI1, GATA1, GFI1B, GP6, GP9, GPIBA, GPIBB, HPS1, HPS3, HPS4, HPS5, HPS6, ITGA2B, ITGB3, LYST, NBEAL2, P2RY12, PLA2G4A, PRKACG, RASGRP2, RUNX1, STIM1, TBXA2R, VIPAS39, VPS33B
This genetic panel is optimized for the detection of germline variants in 31 genes known to cause inherited platelet function disorders.
Additional Test Information
Amniotic Fluid, Buccal Swabs, Cultured Amniocytes, CVS, DNA, EDTA Bone Marrow, EDTA Whole Blood
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
Capture hybridization and Next Generation Sequencing (miSeq) with supplementary Sanger for quality and coverage