List of variants in gene ENAM reported as likely benign for tooth hard tissue disease

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_031889.3(ENAM):c.*1500G>A	rs72654391	0.02266
NM_031889.3(ENAM):c.*936T>A	rs115766831	0.02004
NM_031889.3(ENAM):c.177G>T (p.Arg59=)	rs2609429	0.01011
NM_031889.3(ENAM):c.1165G>A (p.Gly389Ser)	rs74511578	0.01007
NM_031889.3(ENAM):c.*256G>A	rs117342040	0.00061

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