ClinVar Miner

Submissions for variant NM_006270.5(RRAS):c.360C>T (p.Gly120=)

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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 RCV005205090 SCV005844590 likely benign Noonan syndrome 2025-01-11 criteria provided, single submitter clinical testing

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