ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.307-10T>C (rs572853043)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000582091 SCV000689875 likely benign Hereditary cancer-predisposing syndrome 2017-08-10 criteria provided, single submitter clinical testing
Counsyl RCV000663206 SCV000786389 likely benign Lynch syndrome II 2018-04-25 criteria provided, single submitter clinical testing
Invitae RCV000119218 SCV000153960 likely benign Lynch syndrome 2014-11-06 no assertion criteria provided clinical testing

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