ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.834+20G>T

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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 RCV003654834 SCV004559212 likely benign RASopathy 2022-10-27 criteria provided, single submitter clinical testing

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