ClinVar Miner

Submissions for variant NM_007373.4(SHOC2):c.1557A>G (p.Leu519=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002794992 SCV003025124 likely benign RASopathy 2022-02-27 criteria provided, single submitter clinical testing

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