ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.253T>C (p.Leu85=)

dbSNP: rs2135266192
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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 RCV002144718 SCV002420733 likely benign RASopathy 2021-08-11 criteria provided, single submitter clinical testing

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