List of variants in gene WDR72 reported as likely benign for dental enamel hypoplasia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_182758.4(WDR72):c.1839G>A (p.Val613=)	rs78493456	0.01140
NM_182758.4(WDR72):c.1437A>C (p.Gln479His)	rs34123953	0.01023
NM_182758.4(WDR72):c.857+9A>C	rs139139066	0.00974
NM_182758.4(WDR72):c.*588G>A	rs140879069	0.00936
NM_182758.4(WDR72):c.*3575T>C	rs193055203	0.00834
NM_182758.4(WDR72):c.*3433G>A	rs13329257	0.00827
NM_182758.4(WDR72):c.*3325G>A	rs74015387	0.00744
NM_182758.4(WDR72):c.*3592A>G	rs111488180	0.00592
NM_182758.4(WDR72):c.*852G>A	rs112576390	0.00577
NM_182758.4(WDR72):c.*2947A>T	rs74015388	0.00572
NM_182758.4(WDR72):c.*647G>A	rs78618140	0.00478
NM_182758.4(WDR72):c.2598A>G (p.Lys866=)	rs115484883	0.00442
NM_182758.4(WDR72):c.*3689A>G	rs74871423	0.00094
NM_182758.4(WDR72):c.2942A>G (p.Gln981Arg)	rs188590145	0.00053
NM_182758.4(WDR72):c.*3734A>G	rs371978233	0.00002
NM_182758.4(WDR72):c.3149-30CT[13]	rs57737580

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