ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.990+16A>G

dbSNP: rs2125380028
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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 RCV002217938 SCV002379912 likely benign RASopathy 2022-11-01 criteria provided, single submitter clinical testing

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