List of variants in gene combination C10orf105, CDH23 reported as benign for auditory system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.4051A>G (p.Asn1351Asp)	rs1227065	0.79969
NM_022124.6(CDH23):c.4206+131T>C	rs1227061	0.77987
NM_022124.6(CDH23):c.4206+61T>A	rs1227062	0.77967
NM_022124.6(CDH23):c.3370-46T>C	rs3802712	0.17108
NM_022124.6(CDH23):c.3580-12C>T	rs73275848	0.05331
NM_022124.6(CDH23):c.3625A>G (p.Thr1209Ala)	rs41281314	0.04612
NM_022124.6(CDH23):c.3664G>A (p.Ala1222Thr)	rs41281316	0.02047
NM_022124.6(CDH23):c.3430+114T>C	rs7893748

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