ClinVar Miner

Submissions for variant NM_030662.4(MAP2K2):c.1101C>G (p.Thr367=)

dbSNP: rs1483599413
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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 RCV002159303 SCV002473519 likely benign RASopathy 2020-11-25 criteria provided, single submitter clinical testing

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