ClinVar Miner

Submissions for variant NM_001040616.3(LINS1):c.718C>T (p.Arg240Trp) (rs145145735)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192421 SCV000247849 benign not specified 2015-10-20 criteria provided, single submitter clinical testing
Ambry Genetics RCV000717980 SCV000848841 likely benign History of neurodevelopmental disorder 2019-03-29 criteria provided, single submitter clinical testing Sub-population frequency in support of benign classification (not ava blue, manual h-w)
Invitae RCV000880506 SCV001023603 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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