ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.349A>G (p.Met117Val)

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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 RCV003063535 SCV003457704 likely benign RASopathy 2022-11-15 criteria provided, single submitter clinical testing

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