List of variants in gene CDH23 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.5237G>A (p.Arg1746Gln)	rs111033270	0.00016
NM_022124.6(CDH23):c.6442G>A (p.Asp2148Asn)	rs111033271	0.00010
NM_022124.6(CDH23):c.9565C>T (p.Arg3189Trp)	rs121908353	0.00003
NM_022124.6(CDH23):c.6344G>A (p.Arg2115His)	rs1270566026	0.00001
NM_022124.6(CDH23):c.719C>T (p.Pro240Leu)	rs121908354	0.00001
NM_022124.6(CDH23):c.7362+5G>A	rs727502931	0.00001
NM_022124.6(CDH23):c.902G>A (p.Arg301Gln)	rs121908355	0.00001
NM_022124.6(CDH23):c.9886G>A (p.Asp3296Asn)	rs372388344	0.00001
NM_022124.6(CDH23):c.193del (p.Leu65fs)	rs796051861
NM_022124.6(CDH23):c.4488G>C (p.Gln1496His)	rs121908347
NM_022124.6(CDH23):c.5663T>C (p.Phe1888Ser)	rs121908352
NM_022124.6(CDH23):c.6133G>A (p.Asp2045Asn)	rs121908348
NM_022124.6(CDH23):c.6604G>A (p.Asp2202Asn)	rs121908349
NM_022124.6(CDH23):c.9412C>T (p.Arg3138Trp)	rs1052484950

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