ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.424-5_424-3del

dbSNP: rs764020787
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813622 SCV002060611 likely benign Noonan syndrome and Noonan-related syndrome 2021-05-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074229 SCV002458267 likely benign RASopathy 2023-08-31 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587216 SCV005077120 benign not specified 2024-04-21 criteria provided, single submitter clinical testing

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