ClinVar Miner

Submissions for variant NM_182758.4(WDR72):c.1766-2423_1962+1074del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dental Genetics Laboratory, Seoul National University School of Dentistry RCV003313812 SCV002820078 pathogenic Amelogenesis imperfecta no assertion criteria provided clinical testing

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