List of variants in gene combination CDH23, PSAP reported as uncertain significance for not provided

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.9629T>C (p.Ile3210Thr)	rs144688588	0.00026
NM_022124.6(CDH23):c.9799C>T (p.Arg3267Cys)	rs201727938	0.00016
NM_022124.6(CDH23):c.9983G>A (p.Arg3328His)	rs148475933	0.00009
NM_022124.6(CDH23):c.9291G>T (p.Lys3097Asn)	rs368441850	0.00006
NM_022124.6(CDH23):c.9860G>A (p.Gly3287Asp)	rs562590210	0.00001
NC_000010.10:g.(?_73574689)_(73610978_?)del
NM_022124.6(CDH23):c.9739-12G>A	rs200638595

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