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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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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)
NM_031889.3(ENAM):c.79C>A (p.Leu27Ile)

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