ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.609-13C>G

dbSNP: rs1803839206
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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 RCV003105019 SCV003783776 likely benign RASopathy 2023-11-28 criteria provided, single submitter clinical testing

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