ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.767_768del (p.Glu256fs)

dbSNP: rs869312780
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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 RCV000210138 SCV000266127 pathogenic Cowden syndrome 2015-11-20 criteria provided, single submitter clinical testing

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