ClinVar Miner

Submissions for variant NM_000077.5(CDKN2A):c.457+929C>T

gnomAD frequency: 0.00011  dbSNP: rs869312793
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Department of Laboratory Medicine, University of Washington RCV000210118 SCV000266164 uncertain significance Hereditary cancer-predisposing syndrome 2015-11-20 criteria provided, single submitter clinical testing

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