List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 18A by Genome-Nilou Lab

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Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_153676.4(USH1C):c.2656-260A>G	rs7108947	0.95611
NM_153676.4(USH1C):c.-183T>G	rs1859819	0.57652
NM_153676.4(USH1C):c.1086-45A>G	rs2041031	0.57266
NM_153676.4(USH1C):c.1086-42G>A	rs2108332	0.57242
NM_153676.4(USH1C):c.1086-108A>G	rs2041032	0.56388
NM_153676.4(USH1C):c.37-45C>G	rs2240489	0.56124
NM_153676.4(USH1C):c.760-66T>C	rs4757539	0.56102
NM_153676.4(USH1C):c.1188A>G (p.Pro396=)	rs2240487	0.51629
NM_153676.4(USH1C):c.2457G>C (p.Glu819Asp)	rs1064074	0.48497
NM_153676.4(USH1C):c.1413+52C>T	rs2190453	0.47939
NM_153676.4(USH1C):c.37-61A>G	rs878546	0.45653
NM_153676.4(USH1C):c.*211A>G	rs1055581	0.45185
NM_153676.4(USH1C):c.*46T>C	rs1055574	0.44023
NM_153676.4(USH1C):c.*186C>T	rs1055577	0.43773
NM_153676.4(USH1C):c.1085+21C>G	rs2240488	0.43168
NM_153676.4(USH1C):c.105-16C>T	rs2041027	0.41822
NM_153676.4(USH1C):c.36+214C>T	rs7125811	0.39120
NM_153676.4(USH1C):c.2656-47C>T	rs2072225	0.38117
NM_153676.4(USH1C):c.2547-11T>C	rs10832795	0.35821
NM_153676.4(USH1C):c.522-45del	rs5789990	0.31188
NM_153676.4(USH1C):c.580-27G>A	rs6486378	0.30297
NM_153676.4(USH1C):c.579+61G>A	rs72870320	0.23593
NM_153676.4(USH1C):c.2340C>T (p.Val780=)	rs10832796	0.21080
NM_153676.4(USH1C):c.1414-34G>A	rs2237964	0.16591
NM_153676.4(USH1C):c.2490+12G>C	rs2072232	0.12422
NM_153676.4(USH1C):c.2381-46G>A	rs2072233	0.10738
NM_153676.4(USH1C):c.37-47G>T	rs2355022	0.09867
NM_153676.4(USH1C):c.2226+197G>A	rs12270644	0.09831
NM_153676.4(USH1C):c.521+56A>G	rs41282940	0.09720
NM_153676.4(USH1C):c.1086-12G>A	rs11024318	0.09048
NM_153676.4(USH1C):c.2226+12C>T	rs17703528	0.05274
NM_153676.4(USH1C):c.2134-12T>C	rs76769358	0.04923
NM_153676.4(USH1C):c.1770C>T (p.Ala590=)	rs17776775	0.03494
NM_153676.4(USH1C):c.1261-34C>T	rs2190454
NM_153676.4(USH1C):c.2546+125A>G	rs2072229
NM_153676.4(USH1C):c.496+33=	rs12795083

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