List of variants reported as not provided for dental enamel hypoplasia

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001142.2(AMELX):c.131G>A (p.Ser44Asn)	rs431825177	0.00001
NM_001142.2(AMELX):c.129G>C (p.Gln43His)	rs431825176
NM_001142.2(AMELX):c.132C>A (p.Ser44Arg)	rs431825178
NM_198488.5(FAM83H):c.2250C>T (p.Gly750=)	rs431825179
NM_198488.5(FAM83H):c.2765G>T (p.Arg922Leu)	rs431825180
NM_198488.5(FAM83H):c.2766C>T (p.Arg922=)	rs431825181

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