ClinVar Miner

Submissions for variant NM_000077.5(CDKN2A):c.90G>T (p.Ala30=)

dbSNP: rs1563892643
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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 RCV002165514 SCV002340835 likely benign Familial melanoma 2022-05-27 criteria provided, single submitter clinical testing

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