ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.219-17G>A

dbSNP: rs767249235
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002203626 SCV002485509 likely benign Familial melanoma 2024-12-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785526 SCV005406971 likely benign Melanoma, cutaneous malignant, susceptibility to, 3 2024-09-25 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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