ClinVar Miner

Submissions for variant NM_005633.3(SOS1):c.587C>T (p.Ser196Leu) (rs199898869)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000213944 SCV000272448 uncertain significance not specified 2017-08-21 criteria provided, single submitter clinical testing proposed classification - variant undergoing re-assessment, contact laboratory
Illumina Clinical Services Laboratory,Illumina RCV000358698 SCV000430447 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000268538 SCV000430448 uncertain significance Gingival fibromatosis 2016-06-14 criteria provided, single submitter clinical testing

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