List of variants in gene CDH3 reported as likely pathogenic for retinal disorder

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_001793.6(CDH3):c.2200G>A (p.Val734Met)	rs775541873	0.00001
NM_001793.6(CDH3):c.2087del (p.Asp696fs)	rs1961688932
NM_001793.6(CDH3):c.3G>A (p.Met1Ile)	rs1238109100

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