List of variants in gene combination FAM20A, PRKAR1A 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)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.928+16G>A	rs16973042	0.01441
NM_017565.4(FAM20A):c.1314C>T (p.His438=)	rs78050433	0.00053
NM_017565.4(FAM20A):c.1472C>T (p.Thr491Ile)	rs182816928	0.00015
NM_017565.4(FAM20A):c.792C>T (p.Ile264=)	rs139591838	0.00014
NM_017565.4(FAM20A):c.984T>C (p.Ala328=)	rs374633547	0.00011

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