ClinVar Miner

List of variants in gene USH2A reported as benign by PreventionGenetics

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Total variants: 27
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HGVS dbSNP
NM_206933.3(USH2A):c.10232A>C (p.Glu3411Ala) rs10864198
NM_206933.3(USH2A):c.10851C>T (p.Asn3617=) rs12073994
NM_206933.3(USH2A):c.11504C>T (p.Thr3835Ile) rs11120616
NM_206933.3(USH2A):c.11602A>G (p.Met3868Val) rs35309576
NM_206933.3(USH2A):c.11736G>A (p.Glu3912=) rs56053654
NM_206933.3(USH2A):c.11907A>T (p.Pro3969=) rs61635304
NM_206933.3(USH2A):c.11946G>A (p.Leu3982=) rs2820718
NM_206933.3(USH2A):c.12666A>G (p.Thr4222=) rs2797234
NM_206933.3(USH2A):c.13191G>A (p.Glu4397=) rs2009923
NM_206933.3(USH2A):c.1419C>T (p.Thr473=) rs1805050
NM_206933.3(USH2A):c.1840+19C>G rs886038764
NM_206933.3(USH2A):c.1931A>T (p.Asp644Val) rs1805048
NM_206933.3(USH2A):c.2109T>C (p.Asp703=) rs45555435
NM_206933.3(USH2A):c.2137G>C (p.Gly713Arg) rs696723
NM_206933.3(USH2A):c.373G>A (p.Ala125Thr) rs10779261
NM_206933.3(USH2A):c.3812-8T>G rs646094
NM_206933.3(USH2A):c.4252-36CTTT[5] rs372388546
NM_206933.3(USH2A):c.504A>G (p.Thr168=) rs4253963
NM_206933.3(USH2A):c.6506T>C (p.Ile2169Thr) rs10864219
NM_206933.3(USH2A):c.6957+19A>G rs6689120
NM_206933.3(USH2A):c.7506G>A (p.Pro2502=) rs12404427
NM_206933.3(USH2A):c.7584C>T (p.Thr2528=) rs78250390
NM_206933.3(USH2A):c.8624G>A (p.Arg2875Gln) rs12118814
NM_206933.3(USH2A):c.8656C>T (p.Leu2886Phe) rs41277200
NM_206933.3(USH2A):c.8937A>G (p.Val2979=) rs139100097
NM_206933.3(USH2A):c.9343A>G (p.Thr3115Ala) rs56032526
NM_206933.3(USH2A):c.9595A>G (p.Asn3199Asp) rs4129843

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