ClinVar Miner

List of variants in gene AMBN reported as likely pathogenic for Amelogenesis imperfecta type 1F

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_016519.6(AMBN):c.295T>C (p.Tyr99His)
NM_016519.6(AMBN):c.571-1G>C
NM_016519.6(AMBN):c.76G>A (p.Ala26Thr)

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