ClinVar Miner

Submissions for variant NM_006912.6(RIT1):c.238-9T>A

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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 RCV003582911 SCV004315036 likely benign Noonan syndrome 8 2023-10-28 criteria provided, single submitter clinical testing

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