ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.2153+14A>C

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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 RCV003655922 SCV004505771 likely benign RASopathy 2023-03-07 criteria provided, single submitter clinical testing

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