ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.633-14C>G

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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 RCV005149248 SCV005778675 likely benign Familial melanoma 2024-10-11 criteria provided, single submitter clinical testing

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