List of variants reported as likely benign for amelogenesis imperfecta type 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_182758.4(WDR72):c.1839G>A (p.Val613=)	rs78493456	0.01309
NM_182758.4(WDR72):c.857+9A>C	rs139139066	0.00959
NM_182758.4(WDR72):c.3149-30CT[13]	rs57737580
NM_182758.4(WDR72):c.965G>A (p.Arg322His)

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