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Color Health's test of 29 genes linked to inherited breast, ovarian, bowel, stomach, pancreatic, prostate and skin cancer risk.
Registered in the NIH Genetic Testing Registry as GTR000558503.6 (updated 29 August 2026) by Color Diagnostics, LLC (doing business as Color Health; CLIA 05D2081492): APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11 and TP53. GTR records it as a test developed by the laboratory; it is not among the FDA-authorised hereditary cancer products.
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Query for this drug: (TITLE:"Color Hereditary Cancer Test" OR ABSTRACT:"Color Hereditary Cancer Test") 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 Color Hereditary Cancer Test, not a curated reading list.
Shares Familial atypical multiple mole melanoma syndrome (familial melanoma), CDH1, CHEK2, MSH2 and the tags test, hereditary.
Shares Juvenile polyposis syndrome, MUTYH, Peutz-Jeghers syndrome, CDH1 and the tags test, hereditary.
Shares CDH1, CHEK2, PALB2, STK11 and the tags test, hereditary.
Shares Peutz-Jeghers 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 MUTYH, Hereditary cancer syndromes, Germline (hereditary) testing and the tags test, hereditary.
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