ClinVar Miner

List of variants reported as pathogenic for Amelogenesis imperfecta - hypoplastic autosomal dominant - local

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_031889.3(ENAM):c.1259_1260insAG (p.Pro422fs) rs587776588 0.00018
NM_031889.3(ENAM):c.123+2T>G rs1553887511
NM_031889.3(ENAM):c.157A>T (p.Lys53Ter) rs121908109
NM_031889.3(ENAM):c.534+1G>A rs587776587
NM_031889.3(ENAM):c.588+1del rs752102959
NM_031889.3(ENAM):c.664C>T (p.Gln222Ter)
NM_031889.3(ENAM):c.92T>G (p.Leu31Arg) rs1060499539

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