ClinVar Miner

List of variants in gene USH2A studied for Hearing impairment

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_206933.4(USH2A):c.14519T>C (p.Leu4840Pro) rs143275144 0.00031
NM_206933.4(USH2A):c.1898C>T (p.Ser633Leu) rs373190681 0.00014
NM_206933.4(USH2A):c.11864G>A (p.Trp3955Ter) rs111033364 0.00012
NM_206933.4(USH2A):c.2035G>A (p.Gly679Arg) rs367693972 0.00009
NM_206933.4(USH2A):c.908G>A (p.Arg303His) rs371777049 0.00004
NM_206933.4(USH2A):c.1585A>C (p.Thr529Pro) rs201332729 0.00003
NM_206933.4(USH2A):c.10058C>T (p.Pro3353Leu) rs755020832 0.00001
NM_206933.4(USH2A):c.12458C>T (p.Ala4153Val) rs779875423 0.00001
NM_206933.4(USH2A):c.2168-1G>C rs748961218 0.00001
NM_206933.4(USH2A):c.5118G>A (p.Trp1706Ter) rs1461319754 0.00001
NM_206933.4(USH2A):c.8730T>A (p.Phe2910Leu) rs373811292 0.00001
NM_206933.4(USH2A):c.1270A>T (p.Met424Leu) rs2102654082
NM_206933.4(USH2A):c.14396C>T (p.Thr4799Ile) rs2102643267
NM_206933.4(USH2A):c.5320T>A (p.Leu1774Met) rs2102554556
NM_206933.4(USH2A):c.5919G>A (p.Val1973=) rs2102546199
NM_206933.4(USH2A):c.8452C>T (p.Pro2818Ser) rs1470809474
NM_206933.4(USH2A):c.9413G>C (p.Gly3138Ala) rs756163056

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