List of variants in gene combination C10orf105, CDH23 reported as likely benign for Usher syndrome type 1

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.3574G>A (p.Val1192Ile)	rs80028391	0.00999
NM_022124.6(CDH23):c.3364T>G (p.Leu1122Val)	rs77821631	0.00732
NM_022124.6(CDH23):c.4045C>T (p.Arg1349Cys)	rs41281318	0.00285
NM_022124.6(CDH23):c.3293A>G (p.Asn1098Ser)	rs41281310	0.00258
NM_022124.6(CDH23):c.3801C>T (p.Thr1267=)	rs56107171	0.00193
NM_022124.6(CDH23):c.3361A>T (p.Ile1121Phe)	rs200542052	0.00124
NM_022124.6(CDH23):c.4095C>T (p.Asp1365=)	rs368582818	0.00028
NM_022124.6(CDH23):c.3431-6A>T	rs377614198	0.00018
NM_022124.6(CDH23):c.3352G>A (p.Gly1118Ser)	rs562052236	0.00009
NM_022124.6(CDH23):c.3924C>T (p.Asp1308=)	rs776501112	0.00003
NM_022124.6(CDH23):c.4011C>A (p.Ala1337=)	rs761003107	0.00001

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