ClinVar Miner

Submissions for variant NM_031889.3(ENAM):c.-61+1G>A

dbSNP: rs2109817825
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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 RCV001615152 SCV001499580 pathogenic Amelogenesis imperfecta no assertion criteria provided clinical testing

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