ClinVar Miner

Submissions for variant NM_000077.5(CDKN2A):c.150+10G>T

dbSNP: rs557891718
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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 RCV002199197 SCV002493452 likely benign Familial melanoma 2021-01-15 criteria provided, single submitter clinical testing

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