List of variants in gene CDH23 reported by University of Washington Center for Mendelian Genomics, University of Washington

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.2263C>T (p.His755Tyr)	rs181255269	0.00078
NM_022124.6(CDH23):c.4892C>T (p.Ala1631Val)	rs370762269	0.00025
NM_022124.6(CDH23):c.2866G>A (p.Glu956Lys)	rs756147087	0.00009
NM_022124.6(CDH23):c.6050-9G>A	rs367928692	0.00006
NM_022124.6(CDH23):c.2968G>A (p.Asp990Asn)	rs771766431	0.00001
NM_022124.6(CDH23):c.7814A>G (p.Asn2605Ser)	rs780917129	0.00001
NM_022124.6(CDH23):c.5149T>C (p.Cys1717Arg)	rs552998089
NM_022124.6(CDH23):c.6049+1G>A	rs111033247
NM_022124.6(CDH23):c.6083A>C (p.Asp2028Ala)	rs762226905
NM_022124.6(CDH23):c.6133G>A (p.Asp2045Asn)	rs121908348
NM_022124.6(CDH23):c.6202A>C (p.Thr2068Pro)	rs762118583
NM_022124.6(CDH23):c.6604G>A (p.Asp2202Asn)	rs121908349
NM_022124.6(CDH23):c.8351_8352insCGAT (p.Leu2785fs)	rs1564805114

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