ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.444-4G>T

dbSNP: rs1331093488
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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 RCV001435573 SCV001638399 likely benign RASopathy 2019-10-21 criteria provided, single submitter clinical testing

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