ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.1833_1843dup (p.His615fs)

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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 syndrome 2008-01-01 no assertion criteria provided literature only
OMIM RCV001794436 SCV000027126 pathogenic Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 2008-01-01 no assertion criteria provided literature only

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