ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1518-5T>C

dbSNP: rs940384157
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704818 SCV000730529 likely benign not provided 2019-11-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060619 SCV002348046 likely benign RASopathy 2022-11-24 criteria provided, single submitter clinical testing

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