ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.2157C>T (p.Arg719=)

dbSNP: rs1796236915
Minimum review status: Collection method:
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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 RCV002183652 SCV002477749 likely benign RASopathy 2023-10-03 criteria provided, single submitter clinical testing

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