ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.683+15T>C

dbSNP: rs2140383719
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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 RCV002093031 SCV002373429 likely benign Familial melanoma 2021-04-11 criteria provided, single submitter clinical testing

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