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
PreventionGenetics,PreventionGenetics RCV000252980 SCV000308856 benign not specified 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 2019-12-31 criteria provided, single submitter clinical testing
Counsyl RCV000662742 SCV000785521 benign Hereditary nonpolyposis colorectal cancer type 8 2017-09-01 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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