ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1178-860T>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003434153 SCV004161138 likely benign not provided 2025-04-01 criteria provided, single submitter clinical testing BRAF: BS1

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