List of variants reported as likely pathogenic for dental enamel hypoplasia by Center of Excellence in Genomics and Precision Dentistry, Faculty of Dentistry, Chulalongkorn University

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000888.5(ITGB6):c.1661-3C>G	rs1683256077
NM_017565.4(FAM20A):c.1231C>T (p.Arg411Trp)	rs149970399
NM_017565.4(FAM20A):c.758A>G (p.Tyr253Cys)	rs2143526006

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