ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.2128-44_2128-18del

dbSNP: rs1562931259
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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 RCV002089490 SCV002328899 likely benign RASopathy 2021-04-14 criteria provided, single submitter clinical testing

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