ClinVar Miner

Submissions for variant NM_005220.3(DLX3):c.92C>G (p.Thr31Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Reference Center For Rare Oral And Dental Diseases, Crmr O-rares, Hôpitaux Universitaires De Strasbourg RCV003154836 SCV003843190 uncertain significance Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism 2023-03-01 criteria provided, single submitter clinical testing

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