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

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_031889.3(ENAM):c.2315C>A (p.Ala772Asp)	rs144070672	0.00018
NM_031889.3(ENAM):c.101T>C (p.Leu34Pro)	rs2545341444
NM_031889.3(ENAM):c.79C>A (p.Leu27Ile)
NM_031889.3(ENAM):c.889G>A (p.Ala297Thr)

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