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Myriad's multi-gene blood test for inherited cancer risk, covering 63 genes including BRCA1, BRCA2 and the Lynch syndrome genes, ordered through a clinician.
Registered in the NIH Genetic Testing Registry as GTR000603556.3 (version updated 15 December 2025) by Myriad Genetics, Inc. (Utah, CLIA 05D2299797 and 46D2275645): next-generation sequencing of 63 genes, among them BRCA1, BRCA2, PALB2, ATM, CHEK2, the Lynch genes, APC, MUTYH, CDH1, CTNNA1, STK11, TP53, PTEN, CDKN2A, FLCN, VHL, the SDH genes and HOXB13. GTR records it as a test developed by the laboratory; it is not among the FDA-authorised hereditary cancer products (openFDA product codes QAZ and QVU and PMA product code PJG, searched 4 November 2026). Myriad's FDA-approved companion diagnostic for germline BRCA is a separate test, BRACAnalysis CDx.
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Query for this drug: (TITLE:"MyRisk Hereditary Cancer" OR ABSTRACT:"MyRisk Hereditary Cancer" OR TITLE:"Myriad Genetics" OR ABSTRACT:"Myriad Genetics" OR TITLE:"MyRisk" OR ABSTRACT:"MyRisk" OR TITLE:"myRisk" OR ABSTRACT:"myRisk" OR TITLE:"myRisk Hereditary Cancer" OR ABSTRACT:"myRisk Hereditary Cancer" OR TITLE:"Myriad myRisk" OR ABSTRACT:"Myriad myRisk") 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 MyRisk Hereditary Cancer (Myriad Genetics), not a curated reading list.
Shares Familial atypical multiple mole melanoma syndrome (familial melanoma), CDH1, CHEK2, MSH2 and the tags test, hereditary.
Shares Hereditary diffuse gastric cancer, CDH1, CHEK2, PALB2 and the tags test, hereditary.
Shares Birt-Hogg-Dubé syndrome, MSH2, MLH1, PALB2 and the tags test, hereditary.
Shares Birt-Hogg-Dubé syndrome, MSH2, MLH1, PALB2 and the tags test, hereditary.
Shares Hereditary diffuse gastric cancer, CDH1, MSH2, MLH1 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 PALB2, Hereditary cancer syndromes, BRCA1 / BRCA2 (HRD), TP53 and the tags test, hereditary.
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