List of variants in gene combination FAM20A, PRKAR1A reported as benign for dental enamel hypoplasia

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: 2

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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

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