List of variants in gene FAM83H reported as benign for amelogenesis imperfecta, type 3A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_198488.5(FAM83H):c.1827C>T (p.Tyr609=)	rs13254035	0.81988
NM_198488.5(FAM83H):c.2884C>T (p.Leu962=)	rs11136321	0.60606
NM_198488.5(FAM83H):c.1493C>T (p.Pro498Leu)	rs1137806	0.11038

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