ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.42T>G (p.Gly14=)

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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 RCV002932663 SCV003260231 likely benign RASopathy 2022-07-26 criteria provided, single submitter clinical testing

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