ClinVar Miner

List of variants in gene CDH23 studied for Autosomal recessive nonsyndromic hearing loss 12; Usher syndrome type 1D

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.7823G>A (p.Arg2608His)	rs202052174	0.00059
NM_022124.6(CDH23):c.5066T>C (p.Met1689Thr)	rs397517334	0.00002
NM_022124.6(CDH23):c.10036G>C (p.Glu3346Gln)	rs562525508

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