ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.726C>T (p.Asp242=)

dbSNP: rs886152926
Minimum review status: Collection method:
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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 RCV002154375 SCV002470661 likely benign RASopathy 2023-12-12 criteria provided, single submitter clinical testing

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