List of variants reported as likely pathogenic for dental enamel hypoplasia by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004917.5(KLK4):c.224+2T>C
NM_182758.4(WDR72):c.1348+1G>T
NM_182758.4(WDR72):c.858-1G>C

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