ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.291A>G (p.Ala97=)

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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 RCV003655517 SCV004383283 likely benign RASopathy 2024-01-11 criteria provided, single submitter clinical testing

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