ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.582-7T>G

dbSNP: rs2125407243
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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 RCV001505496 SCV001710402 likely benign RASopathy 2019-03-22 criteria provided, single submitter clinical testing

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