Single-gene assays
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.
Single-gene assays test menu
Single-gene assays
Key testing
- BHDZ | Birt-Hogg-Dube Syndrome, FLCN, Full Gene Analysis, Varies
- Identifies variants within genes known to be associated with increased risk for Birt-Hogg-Dube syndrome, allowing for predictive testing of at-risk family members.
- BAP1Z | BAP1-Tumor Predisposition Syndrome, BAP1 Full Gene Analysis, Varies
- Identifies genetic variants associated with increased risk for BAP1-tumor predisposition syndrome, 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 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.
- 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.