ClinVar Miner

Submissions for variant NM_002834.5(PTPN11):c.1712+11C>T

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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 RCV002720193 SCV002993048 likely benign RASopathy 2021-12-21 criteria provided, single submitter clinical testing

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