List of variants reported as likely benign for primary failure of tooth eruption

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000316.3(PTH1R):c.1395+15G>A	rs151077141	0.00747
NM_000316.3(PTH1R):c.216G>A (p.Ala72=)	rs116789130	0.00466
NM_000316.3(PTH1R):c.128G>A (p.Arg43His)	rs141466964	0.00237
NM_000316.3(PTH1R):c.75+12G>A	rs200603325	0.00081
NM_000316.3(PTH1R):c.375G>A (p.Glu125=)	rs138339848	0.00034
NM_000316.3(PTH1R):c.1212-18C>T	rs200401411	0.00008
NM_000316.3(PTH1R):c.1254C>T (p.Gly418=)	rs750736467	0.00006
NM_000316.3(PTH1R):c.1396-19G>A	rs370461607	0.00003
NM_000316.3(PTH1R):c.1117-8T>C	rs749389822	0.00001
NM_000316.3(PTH1R):c.615T>C (p.Ala205=)	rs200829369	0.00001
NM_000316.3(PTH1R):c.638+12G>A	rs375241177
NM_000316.3(PTH1R):c.638+12G>C	rs375241177
NM_000316.3(PTH1R):c.771C>A (p.Thr257=)	rs201016660

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