ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.504+17A>G

gnomAD frequency: 0.00013  dbSNP: rs201797624
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251442 SCV000310115 likely benign not specified criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000251442 SCV002014944 benign not specified 2021-10-17 criteria provided, single submitter clinical testing
Invitae RCV002058154 SCV002397040 benign RASopathy 2024-01-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002262890 SCV002545572 benign not provided 2022-11-01 criteria provided, single submitter clinical testing BRAF: BS1, BS2

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