ClinVar Miner

Submissions for variant NM_002354.2(EPCAM):c.859-7C>T (rs72882786)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662742 SCV000785521 benign Hereditary nonpolyposis colorectal cancer type 8 2017-09-01 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000324490 SCV000430887 likely benign Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000524491 SCV000561822 benign Hereditary nonpolyposis colon cancer 2017-06-01 criteria provided, single submitter clinical testing
PreventionGenetics RCV000252980 SCV000308856 benign not specified criteria provided, single submitter clinical testing
True Health Diagnostics RCV000664271 SCV000788013 likely benign Hereditary cancer-predisposing syndrome 2018-01-03 no assertion criteria provided clinical testing

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