List of variants in gene CDH3 reported as pathogenic for perceptual disorders

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001793.6(CDH3):c.1086G>A (p.Trp362Ter)	rs779888126	0.00001
NM_001793.6(CDH3):c.1508G>A (p.Arg503His)	rs121434542	0.00001
NM_001793.6(CDH3):c.160+1G>A	rs1474181679	0.00001
NM_001793.6(CDH3):c.1183-2A>G
NM_001793.6(CDH3):c.1519C>T (p.Gln507Ter)	rs1961376390
NM_001793.6(CDH3):c.1837dup (p.Asp613fs)	rs1157340043
NM_001793.6(CDH3):c.307C>T (p.Arg103Ter)	rs1157108621
NM_001793.6(CDH3):c.692-1G>T
NM_001793.6(CDH3):c.830del (p.Gly277fs)	rs724159985
NM_001793.6(CDH3):c.965A>T (p.Asn322Ile)	rs121434543

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