List of variants in gene combination CDH23, PSAP studied for Usher syndrome type 1

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.9873G>A (p.Thr3291=)	rs2290021	0.08719
NM_022124.6(CDH23):c.9373T>C (p.Phe3125Leu)	rs45583140	0.04021
NM_022124.6(CDH23):c.9978C>T (p.Asn3326=)	rs73277900	0.02056
NM_022124.6(CDH23):c.9758A>C (p.Asp3253Ala)	rs140463385	0.00447
NM_022124.6(CDH23):c.9510+13C>T	rs183692794	0.00379
NM_022124.6(CDH23):c.9903C>T (p.Pro3301=)	rs55717455	0.00341
NM_022124.6(CDH23):c.9501G>A (p.Thr3167=)	rs144906721	0.00292
NM_022124.6(CDH23):c.10026C>T (p.Asp3342=)	rs377118941	0.00185
NM_022124.6(CDH23):c.9942G>A (p.Thr3314=)	rs376804660	0.00053
NM_022124.6(CDH23):c.9629T>C (p.Ile3210Thr)	rs144688588	0.00026
NM_022124.6(CDH23):c.9983G>A (p.Arg3328His)	rs148475933	0.00009
NM_022124.6(CDH23):c.9860G>A (p.Gly3287Asp)	rs562590210	0.00001
NM_022124.6(CDH23):c.9510+19_9510+25del	rs149704197

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