ClinVar Miner

List of variants in gene USH2A reported as benign by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_206933.3(USH2A):c.3531T>C (p.Gly1177=) rs149570469
NM_206933.4(USH2A):c.10836C>A (p.Val3612=) rs61276761
NM_206933.4(USH2A):c.11677C>A (p.Pro3893Thr) rs41303285
NM_206933.4(USH2A):c.11736G>A (p.Glu3912=) rs56053654
NM_206933.4(USH2A):c.11794C>T (p.Leu3932=) rs111033505
NM_206933.4(USH2A):c.11907A>T (p.Pro3969=) rs61635304
NM_206933.4(USH2A):c.12743A>G (p.His4248Arg) rs145830318
NM_206933.4(USH2A):c.13297G>T (p.Val4433Leu) rs111033381
NM_206933.4(USH2A):c.13984C>G (p.Gln4662Glu) rs41302237
NM_206933.4(USH2A):c.14226G>A (p.Thr4742=) rs78576418
NM_206933.4(USH2A):c.1434G>C (p.Glu478Asp) rs35730265
NM_206933.4(USH2A):c.14481C>T (p.Ala4827=) rs41304083
NM_206933.4(USH2A):c.14513G>A (p.Gly4838Glu) rs41315587
NM_206933.4(USH2A):c.15091C>T (p.Arg5031Trp) rs56038610
NM_206933.4(USH2A):c.15428G>A (p.Arg5143His) rs111033435
NM_206933.4(USH2A):c.15522T>C (p.Tyr5174=) rs77792891
NM_206933.4(USH2A):c.2109T>C (p.Asp703=) rs45555435
NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg) rs696723
NM_206933.4(USH2A):c.3648C>T (p.Tyr1216=) rs147947402
NM_206933.4(USH2A):c.3945T>C (p.Asn1315=) rs41303257
NM_206933.4(USH2A):c.4560C>T (p.Ile1520=) rs148000219
NM_206933.4(USH2A):c.6369C>T (p.Cys2123=) rs111033472
NM_206933.4(USH2A):c.6587G>C (p.Ser2196Thr) rs79444516
NM_206933.4(USH2A):c.6713A>C (p.Glu2238Ala) rs41277212
NM_206933.4(USH2A):c.6875G>A (p.Arg2292His) rs41277210
NM_206933.4(USH2A):c.688G>A (p.Val230Met) rs45500891
NM_206933.4(USH2A):c.7685T>C (p.Val2562Ala) rs56385601
NM_206933.4(USH2A):c.8624G>A (p.Arg2875Gln) rs12118814
NM_206933.4(USH2A):c.9213G>A (p.Ser3071=) rs111033397
NM_206933.4(USH2A):c.9296A>G (p.Asn3099Ser) rs41277194
NM_206933.4(USH2A):c.9430G>A (p.Asp3144Asn) rs11120645

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