List of variants reported as pathogenic for dental enamel hypoplasia by Institute of Human Genetics, University of Ulm

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_182758.4(WDR72):c.2686C>T (p.Arg896Ter)	rs557128345	0.00001
NM_017565.4(FAM20A):c.188dup (p.Asp63fs)
NM_153646.4(SLC24A4):c.1192C>T (p.Gln398Ter)	rs1595312054

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