ClinVar Miner

Submissions for variant NM_058195.4(CDKN2A):c.76C>T (p.His26Tyr)

dbSNP: rs1820533255
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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 RCV001225857 SCV001398151 uncertain significance Familial melanoma 2021-07-14 criteria provided, single submitter clinical testing

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