ClinVar Miner

Submissions for variant NM_001040616.3(LINS1):c.2119G>A (p.Gly707Arg) (rs74039425)

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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 RCV000117491 SCV000151709 benign not specified 2015-11-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV000717667 SCV000848522 uncertain significance History of neurodevelopmental disorder 2019-06-06 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
Invitae RCV000904791 SCV001049334 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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