ClinVar Miner

Submissions for variant NM_000077.5(CDKN2A):c.30G>A (p.Glu10=)

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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 RCV002806684 SCV003195871 likely benign Familial melanoma 2024-02-19 criteria provided, single submitter clinical testing

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