{"entity":{"id":"color-hereditary-cancer-test","kind":"drug","name":"Color Hereditary Cancer Test","aka":[],"tldr":"Color Health's test of 29 genes linked to inherited breast, ovarian, bowel, stomach, pancreatic, prostate and skin cancer risk.","summary":"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.","status":"established","asOf":"2026-11-04","links":[{"label":"NIH Genetic Testing Registry GTR000558503.6","url":"https://www.ncbi.nlm.nih.gov/gtr/tests/558503/"},{"label":"NIH Genetic Testing Registry data file (test_version.gz)","url":"https://ftp.ncbi.nlm.nih.gov/pub/GTR/data/test_version.gz"}],"tags":["test","hereditary"],"related":[],"cancers":[],"sections":[],"technologies":["germline-testing"],"targets":["brca","palb2","atm","chek2","mlh1","msh2","cdh1","stk11","mutyh","cdkn2a","tp53"],"drugs":[],"companies":["color-health"],"institutions":[],"pathways":[],"terms":["hereditary-cancer-syndromes","lynch-syndrome","peutz-jeghers-syndrome","juvenile-polyposis-syndrome","familial-atypical-multiple-mole-melanoma"],"trials":[],"people":[],"bottlenecks":[],"keyPapers":[],"journals":[],"dependsOn":[],"notes":[],"brand":"Color Hereditary Cancer Test","modality":"Germline hereditary cancer sequencing panel (laboratory-developed test)","mechanism":"Next-generation sequencing of 29 hereditary cancer genes in germline DNA.","approvals":[],"mechanismSteps":[],"toxicity":[],"access":[],"regulatoryEvents":[]},"route":"/drugs/color-hereditary-cancer-test/","neighbours":{"technology":[{"id":"germline-testing","kind":"technology","name":"Germline (hereditary) testing","route":"/technologies/germline-testing/"}],"target":[{"id":"atm","kind":"target","name":"ATM","route":"/targets/atm/"},{"id":"brca","kind":"target","name":"BRCA1 / BRCA2 (HRD)","route":"/targets/brca/"},{"id":"cdh1","kind":"target","name":"CDH1","route":"/targets/cdh1/"},{"id":"cdkn2a","kind":"target","name":"CDKN2A","route":"/targets/cdkn2a/"},{"id":"chek2","kind":"target","name":"CHEK2","route":"/targets/chek2/"},{"id":"mlh1","kind":"target","name":"MLH1","route":"/targets/mlh1/"},{"id":"msh2","kind":"target","name":"MSH2","route":"/targets/msh2/"},{"id":"mutyh","kind":"target","name":"MUTYH","route":"/targets/mutyh/"},{"id":"palb2","kind":"target","name":"PALB2","route":"/targets/palb2/"},{"id":"stk11","kind":"target","name":"STK11","route":"/targets/stk11/"},{"id":"tp53","kind":"target","name":"TP53","route":"/targets/tp53/"}],"company":[{"id":"color-health","kind":"company","name":"Color Health","route":"/companies/color-health/"}],"term":[{"id":"familial-atypical-multiple-mole-melanoma","kind":"term","name":"Familial atypical multiple mole melanoma syndrome (familial melanoma)","route":"/terms/familial-atypical-multiple-mole-melanoma/"},{"id":"hereditary-cancer-syndromes","kind":"term","name":"Hereditary cancer syndromes","route":"/terms/hereditary-cancer-syndromes/"},{"id":"juvenile-polyposis-syndrome","kind":"term","name":"Juvenile polyposis syndrome","route":"/terms/juvenile-polyposis-syndrome/"},{"id":"lynch-syndrome","kind":"term","name":"Lynch syndrome","route":"/terms/lynch-syndrome/"},{"id":"peutz-jeghers-syndrome","kind":"term","name":"Peutz-Jeghers syndrome","route":"/terms/peutz-jeghers-syndrome/"}]}}