ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.1914A>G (p.Gly638=)

dbSNP: rs2135310998
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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 RCV002178057 SCV002346700 likely benign RASopathy 2022-06-27 criteria provided, single submitter clinical testing

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