ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.1686C>A (p.Gly562=)

gnomAD frequency: 0.00001  dbSNP: rs894831042
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001446943 SCV001649997 likely benign RASopathy 2016-05-17 criteria provided, single submitter clinical testing

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