Comprehensive Hereditary Cancer Panel

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50-Gene Hereditary Cancer Panel

A comprehensive genetic test assessing 50 genes associated with inherited cancer predisposition and hereditary tumor syndromes.

Genes included:
ATM • APC • BARD1 • BRCA1 • BRCA2 • BRIP1 • CDH1 • CHEK2 • EPCAM • FAM175A • MLH1 • MRE11A • MSH2 • MSH6 • MUTYH • NBN • PALB2 • PIK3CA • PMS2 • PMS2CL • PTEN • RAD50 • RAD51C • RAD51D • STK11 • TP53 • XRCC2 • NF1 • SPRED1 • MEN1 • RET • SMARCB1 • NF2 • LZTR1C • TNNB1 • KRAS • ERBB2 • ALK • EGFR • RB1 • CDKN2A • CDK4 • FLCN • RUNX1 • XPC • WRN • PTCH1 • CDKN1C • SMAD4 • HRAS

Associated hereditary cancer syndromes & predispositions:

• Breast & ovarian cancer
• Hereditary colorectal cancer & polyposis
• Lynch syndrome
• Li-Fraumeni syndrome
• Cowden syndrome 
• Peutz-Jeghers syndrome
• Muir-Torre syndrome
• Gardner syndrome
• Multiple endocrine neoplasia (MEN)
• Hereditary diffuse gastric cancer
• Melanoma-pancreatic cancer syndrome
• Retinoblastoma 
• Rhabdoid tumor 
• Fanconi anemia
• Hereditary prostate cancer 
• Hereditary thyroid cancer
• Hereditary leukemia
• Hereditary melanoma
• Hereditary lung and other solid-tumor