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Quest Diagnostics' test of 66 genes linked to inherited cancer risk, ordered through a clinician.
Registered in the NIH Genetic Testing Registry as GTR000592394.4 (updated 25 June 2024) by Quest Diagnostics Nichols Institute San Juan Capistrano (CLIA 05D0643352), order code 38600: 66 genes, including the Fanconi genes FANCA, FANCC and FANCM, BLM, NTHL1, POLE, POLD1, FLCN, MET, PTCH1 and SUFU alongside the breast, ovarian and Lynch genes. GTR does not record a development type for this entry; it is not among the FDA-authorised hereditary cancer products.
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Query for this drug: (TITLE:"Quest Comprehensive Hereditary Cancer Panel" OR ABSTRACT:"Quest Comprehensive Hereditary Cancer Panel" OR TITLE:"66 genes" OR ABSTRACT:"66 genes" OR TITLE:"Comprehensive Hereditary Cancer Panel" OR ABSTRACT:"Comprehensive Hereditary Cancer Panel") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Quest Comprehensive Hereditary Cancer Panel (66 genes), not a curated reading list.
Shares Birt-Hogg-Dubé syndrome, FLCN, MSH2, MLH1 and the tags test, hereditary.
Shares Birt-Hogg-Dubé syndrome, MSH2, MLH1, PALB2 and the tags test, hereditary.
Shares MSH2, MLH1, PALB2, Lynch syndrome and the tags test, hereditary.
Shares MSH2, MLH1, Lynch syndrome, Hereditary cancer syndromes and the tags test, hereditary.
Shares MSH2, MLH1, PALB2, Lynch syndrome and the tags test, hereditary.
Shares MSH2, MLH1, PALB2, Lynch syndrome and the tags test, hereditary.
Shares Hereditary cancer syndromes, BRCA1 / BRCA2 (HRD), Germline (hereditary) testing and the tags test, hereditary.
Shares PALB2, Hereditary cancer syndromes, BRCA1 / BRCA2 (HRD), Germline (hereditary) testing and the tags test, hereditary.
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