ClinVar Miner

List of variants reported as benign for Amelogenesis imperfecta type 1G

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.1589T>C (p.Leu530Ser)	rs2907373	0.72701
NM_017565.4(FAM20A):c.996C>A (p.Asn332Lys)	rs2302234	0.30437
NM_017565.4(FAM20A):c.444C>T (p.Ser148=)	rs139743735	0.00235

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