ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.1193+13C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003073495 SCV003477032 likely benign RASopathy 2022-04-17 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003324073 SCV004029456 uncertain significance not specified 2023-07-16 criteria provided, single submitter clinical testing

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