ClinVar Miner

Submissions for variant TP63, 11-BP DUP, NT1716

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000006929 SCV000027125 pathogenic Rapp-Hodgkin ectodermal dysplasia syndrome 2008-01-01 no assertion criteria provided literature only
OMIM RCV000006930 SCV000027126 pathogenic Ankyloblepharon-ectodermal defects, cleft lip/palate 2008-01-01 no assertion criteria provided literature only

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