List of variants in gene CDH23 reported as likely benign by Genome-Nilou Lab

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.624+64C>T	rs7087735	0.34986
NM_022124.6(CDH23):c.1987-123G>A	rs1227087	0.26320
NM_022124.6(CDH23):c.4846-79G>A	rs41281328	0.13922
NM_022124.6(CDH23):c.7762G>C (p.Glu2588Gln)	rs41281338	0.00677
NM_022124.6(CDH23):c.8980-14C>A	rs45522532	0.00642
NM_022124.6(CDH23):c.5544C>T (p.Asp1848=)	rs142131750	0.00488
NM_022124.6(CDH23):c.3074G>A (p.Gly1025Asp)	rs143179070	0.00358
NM_022124.6(CDH23):c.2970C>T (p.Asp990=)	rs56216952	0.00289
NM_022124.6(CDH23):c.1307G>A (p.Ser436Asn)	rs111033369	0.00248
NM_022124.6(CDH23):c.6918G>A (p.Leu2306=)	rs146819206	0.00063
NM_022124.6(CDH23):c.1078C>T (p.Leu360=)	rs185917383	0.00048
NM_022124.6(CDH23):c.1814C>T (p.Ala605Val)	rs201475055	0.00029
NM_022124.6(CDH23):c.2235C>T (p.Ile745=)	rs368841307	0.00012
NM_022124.6(CDH23):c.5026G>A (p.Ala1676Thr)	rs56043301	0.00009
NM_022124.6(CDH23):c.1472C>T (p.Thr491Ile)	rs397517307	0.00002
NM_022124.6(CDH23):c.4589C>T (p.Pro1530Leu)	rs554938323	0.00002

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