List of variants in gene ACP4 reported as likely pathogenic for Amelogenesis imperfecta, type 1J

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_033068.3(ACP4):c.331C>T (p.Arg111Cys)	rs202073531	0.00011
NM_033068.3(ACP4):c.645+1G>A	rs1212633515	0.00001
NM_033068.3(ACP4):c.736G>A (p.Val246Met)	rs756274541	0.00001

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