ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.2128-5T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003654777 SCV004534547 likely benign RASopathy 2023-04-28 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003956535 SCV004778115 likely benign BRAF-related disorder 2022-10-12 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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