List of variants reported as likely benign for tooth hard tissue disease by Fulgent Genetics, Fulgent Genetics

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.640+11T>C	rs8071830	0.02884
NM_017565.4(FAM20A):c.928+16G>A	rs16973042	0.01441
NM_017565.4(FAM20A):c.18G>A (p.Arg6=)	rs75228334	0.01179
NM_182758.4(WDR72):c.1839G>A (p.Val613=)	rs78493456	0.01140
NM_182758.4(WDR72):c.857+9A>C	rs139139066	0.00974
NM_017565.4(FAM20A):c.1314C>T (p.His438=)	rs78050433	0.00053
NM_017565.4(FAM20A):c.513T>C (p.His171=)	rs181817943	0.00030
NM_017565.4(FAM20A):c.43C>T (p.Leu15=)	rs372862593	0.00020
NM_017565.4(FAM20A):c.1472C>T (p.Thr491Ile)	rs182816928	0.00015
NM_017565.4(FAM20A):c.792C>T (p.Ile264=)	rs139591838	0.00014
NM_017565.4(FAM20A):c.404+18G>A	rs773191671	0.00011
NM_017565.4(FAM20A):c.984T>C (p.Ala328=)	rs374633547	0.00011
NM_017565.4(FAM20A):c.321G>C (p.Pro107=)	rs568029338	0.00007
NM_017565.4(FAM20A):c.342C>T (p.Asp114=)	rs778101746	0.00006
NM_017565.4(FAM20A):c.195C>T (p.Gly65=)
NM_182758.4(WDR72):c.3149-30CT[13]	rs57737580
NM_182758.4(WDR72):c.965G>A (p.Arg322His)

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