List of variants in gene CDH23, LOC111982869 studied for nonsyndromic genetic hearing loss

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.8022G>A (p.Gln2674=)	rs201733315	0.00539
NM_022124.6(CDH23):c.7999G>C (p.Asp2667His)	rs200251748	0.00009
NM_022124.6(CDH23):c.7942G>A (p.Val2648Met)	rs749501038	0.00004
NM_022124.6(CDH23):c.8062A>G (p.Ser2688Gly)	rs754761193	0.00004
NM_022124.6(CDH23):c.8064+13C>A	rs374981343	0.00004
NM_022124.6(CDH23):c.8009G>A (p.Ser2670Asn)	rs749342092	0.00003
NM_022124.6(CDH23):c.7903G>T (p.Val2635Phe)	rs763721044	0.00002
NM_022124.6(CDH23):c.8012G>A (p.Gly2671Asp)	rs779222449	0.00001
NM_022124.6(CDH23):c.7987TTC[1] (p.Phe2664del)	rs774559018
NM_022124.6(CDH23):c.8061C>G (p.Tyr2687Ter)	rs1564803868

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