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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