ClinVar Miner

Submissions for variant NM_005633.3(SOS1):c.3022T>C (p.Tyr1008His) (rs397517163)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000038544 SCV000062222 likely pathogenic Noonan syndrome 2008-03-01 criteria provided, single submitter clinical testing

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