List of variants in gene PCDH15 reported as 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001384140.1(PCDH15):c.706-8C>T	rs10740579	0.71606
NM_001384140.1(PCDH15):c.1263T>C (p.Thr421=)	rs7921598	0.23801
NM_001384140.1(PCDH15):c.1138G>A (p.Gly380Ser)	rs10825269	0.22813
NM_001384140.1(PCDH15):c.2786G>A (p.Arg929Gln)	rs2135720	0.22399
NM_001384140.1(PCDH15):c.55T>G (p.Ser19Ala)	rs11004439	0.20535
NM_001384140.1(PCDH15):c.1304A>C (p.Asp435Ala)	rs4935502	0.15952
NM_033056.4(PCDH15):c.4581C>A (p.Pro1527=)	rs10825114	0.12444
NM_033056.4(PCDH15):c.5707A>G (p.Ile1903Val)	rs79854148	0.03803
NM_001384140.1(PCDH15):c.4368-1214G>C	rs16937780	0.03481
NM_001384140.1(PCDH15):c.1910A>G (p.Asn637Ser)	rs61731389	0.02908
NM_001384140.1(PCDH15):c.960A>G (p.Pro320=)	rs41274634	0.02389
NM_001384140.1(PCDH15):c.3374-4C>T	rs111739360	0.02123
NM_001384140.1(PCDH15):c.3795A>T (p.Glu1265Asp)	rs111033496	0.01533
NM_001384140.1(PCDH15):c.4368-1207C>T	rs74134797	0.01267
NM_001384140.1(PCDH15):c.1360G>A (p.Val454Ile)	rs61735473	0.00870
NM_001384140.1(PCDH15):c.-5A>G	rs142016527	0.00570
NM_033056.4(PCDH15):c.5286T>A (p.Pro1762=)	rs58461416	0.00220

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