ClinVar Miner

Submissions for variant NM_030662.4(MAP2K2):c.508C>T (p.Leu170=)

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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 RCV002848113 SCV003225671 likely benign RASopathy 2023-07-29 criteria provided, single submitter clinical testing

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