ClinVar Miner

Submissions for variant NM_002834.5(PTPN11):c.933+7T>G

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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 RCV003655586 SCV004393829 likely benign RASopathy 2023-04-17 criteria provided, single submitter clinical testing

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