ClinVar Miner

List of variants in gene USH2A reported as benign by GeneDx

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Gene type:
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Total variants: 75
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HGVS dbSNP
NM_206933.3(USH2A):c.10183-260A>C
NM_206933.3(USH2A):c.10232A>C (p.Glu3411Ala) rs10864198
NM_206933.3(USH2A):c.10585+143A>C
NM_206933.3(USH2A):c.10585+211A>G
NM_206933.3(USH2A):c.10585+267A>G
NM_206933.3(USH2A):c.10851C>T (p.Asn3617=) rs12073994
NM_206933.3(USH2A):c.11048-275G>A
NM_206933.3(USH2A):c.11231+259A>C
NM_206933.3(USH2A):c.11389+233A>G
NM_206933.3(USH2A):c.11389+9A>T rs12095085
NM_206933.3(USH2A):c.11390-52AT[9]
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.11677C>A (p.Pro3893Thr) rs41303285
NM_206933.3(USH2A):c.11712-261C>A
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.11928G>A (p.Thr3976=) rs55961436
NM_206933.3(USH2A):c.11946G>A (p.Leu3982=) rs2820718
NM_206933.3(USH2A):c.12093C>T (p.Tyr4031=) rs55921307
NM_206933.3(USH2A):c.12612G>A (p.Thr4204=) rs2797235
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.13763C>A (p.Ser4588Tyr) rs78253373
NM_206933.3(USH2A):c.13811+72G>A
NM_206933.3(USH2A):c.13984C>G (p.Gln4662Glu) rs41302237
NM_206933.3(USH2A):c.1419C>T (p.Thr473=) rs1805050
NM_206933.3(USH2A):c.1434G>C (p.Glu478Asp) rs35730265
NM_206933.3(USH2A):c.14481C>T (p.Ala4827=) rs41304083
NM_206933.3(USH2A):c.14513G>A (p.Gly4838Glu) rs41315587
NM_206933.3(USH2A):c.14517G>A (p.Thr4839=) rs397517991
NM_206933.3(USH2A):c.14543G>A (p.Arg4848Gln) rs77211159
NM_206933.3(USH2A):c.15076A>G (p.Lys5026Glu) rs41308435
NM_206933.3(USH2A):c.15091C>T (p.Arg5031Trp) rs56038610
NM_206933.3(USH2A):c.15377T>C (p.Ile5126Thr) rs111033266
NM_206933.3(USH2A):c.15428G>A (p.Arg5143His) rs111033435
NM_206933.3(USH2A):c.15522T>C (p.Tyr5174=) rs77792891
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.2168-282C>A
NM_206933.3(USH2A):c.2810-294G>T
NM_206933.3(USH2A):c.3157+254G>A
NM_206933.3(USH2A):c.3364T>G (p.Ser1122Ala) rs148135241
NM_206933.3(USH2A):c.373G>A (p.Ala125Thr) rs10779261
NM_206933.3(USH2A):c.3812-8T>G rs646094
NM_206933.3(USH2A):c.3945T>C (p.Asn1315=) rs41303257
NM_206933.3(USH2A):c.4252-36CTTT[5] rs372388546
NM_206933.3(USH2A):c.4371G>A (p.Ser1457=) rs56013136
NM_206933.3(USH2A):c.4440C>T (p.Ser1480=) rs111632670
NM_206933.3(USH2A):c.4457A>G (p.Lys1486Arg) rs1805049
NM_206933.3(USH2A):c.4628-63C>T
NM_206933.3(USH2A):c.4714C>T (p.Leu1572Phe) rs111033333
NM_206933.3(USH2A):c.504A>G (p.Thr168=) rs4253963
NM_206933.3(USH2A):c.6236A>C (p.Lys2079Thr) rs147039836
NM_206933.3(USH2A):c.6257C>A (p.Thr2086Asn) rs149202379
NM_206933.3(USH2A):c.6317C>T (p.Thr2106Ile) rs6657250
NM_206933.3(USH2A):c.6506T>C (p.Ile2169Thr) rs10864219
NM_206933.3(USH2A):c.6713A>C (p.Glu2238Ala) rs41277212
NM_206933.3(USH2A):c.6875G>A (p.Arg2292His) rs41277210
NM_206933.3(USH2A):c.688G>A (p.Val230Met) rs45500891
NM_206933.3(USH2A):c.6957+19A>G rs6689120
NM_206933.3(USH2A):c.7300+43C>T
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.7594+128C>A
NM_206933.3(USH2A):c.7595-1906T>A
NM_206933.3(USH2A):c.8681+18A>G rs41277198
NM_206933.3(USH2A):c.8845+382A>G
NM_206933.3(USH2A):c.9213G>A (p.Ser3071=) rs111033397
NM_206933.3(USH2A):c.9262G>A (p.Glu3088Lys) rs56056328
NM_206933.3(USH2A):c.9343A>G (p.Thr3115Ala) rs56032526
NM_206933.3(USH2A):c.9371+245C>T
NM_206933.3(USH2A):c.9595A>G (p.Asn3199Asp) rs4129843
NM_206933.3(USH2A):c.9958+246A>C
NM_206933.3(USH2A):c.9958+4171T>C

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