ClinVar Miner

Submissions for variant NM_000077.5(CDKN2A):c.*6C>G

gnomAD frequency: 0.00002  dbSNP: rs375628411
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000985666 SCV000528899 likely benign not provided 2020-11-12 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000579714 SCV000684503 benign Hereditary cancer-predisposing syndrome 2016-10-09 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000985666 SCV001134099 benign not provided 2023-08-23 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002469149 SCV002766588 benign not specified 2022-11-19 criteria provided, single submitter clinical testing

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