ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.1086T>C (p.Thr362=)

dbSNP: rs11549991
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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 RCV002177844 SCV002347865 likely benign RASopathy 2021-04-05 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004526906 SCV005039139 likely benign not specified 2024-03-25 criteria provided, single submitter clinical testing

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