Single gene evaluations    

Tailored testing for genetic associations

When a patient receives a cancer diagnosis or presents with features that point to a single hereditary cancer syndrome, single gene analysis can pinpoint whether the disease is genetic in nature. 

Which test should I order?

BHDZ  | Birt-Hogg-Dube Syndrome, FLCN, Full Gene Analysis, Varies

  • Identifying variants within genes known to be associated with increased risk for BHD syndrome allowing for predictive testing of at-risk family members

BAP1Z | BAP1-Tumor Predisposition Syndrome, BAP1 Full Gene Analysis, Varies

  • Identifying genetic variants associated with increased risk for BAP1-TPDS, allowing for predictive testing and appropriate screening of at-risk family members

CDHZ | Hereditary Diffuse Gastric Cancer Syndrome, CDH1, Full Gene Analysis, Varies

  • Evaluation for patients with a personal or family history suggestive of hereditary diffuse gastric cancer (HDGC) syndrome

LRCCZ | Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome, FH, Full Gene Analysis, Varies

  • Helps identify patients with hereditary leiomyomatosis and renal cell cancer syndrome

NF1Z | Neurofibromatosis Type 1, NF1, Full Gene Analysis, Varies

  • Helps identify patients with neurofibromatosis type 1

PTNZ  | PTEN Hamartoma Tumor Syndrome, PTEN Full Gene Analysis, Varies

  • Helps identify patients with PTEN hamartoma tumor syndrome

RETZZ  | Multiple Endocrine Neoplasia Type 2 Syndrome, RET, Full Gene Analysis, Varies

  • Helps identify patients with multiple endocrine neoplasia type 2

STK1Z   | Peutz-Jeghers Syndrome, STK11, Full Gene Analysis, Varies

  • Helps identify patients with Peutz-Jeghers syndrome

VHLZZ | Von Hippel Lindau Syndrome, VHL, Full Gene Analysis, Varies

  • Helps identify patients with Von Hippel-Lindau syndrome

Learn more about how to order these tests at your institution.