ClinVar Miner

List of variants in gene USH1G reported as likely benign for Usher syndrome type 1

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_173477.5(USH1G):c.*1303C>T rs1013013 0.20471
NM_173477.5(USH1G):c.*1093= rs690566 0.19308
NM_173477.5(USH1G):c.*1656T>C rs8067775 0.06899
NM_173477.5(USH1G):c.*571T>A rs111611253 0.04134
NM_173477.5(USH1G):c.*553A>C rs111899313 0.02634
NM_173477.5(USH1G):c.*1224A>C rs111922548 0.02392
NM_173477.5(USH1G):c.*1053G>A rs113583471 0.00727
NM_173477.5(USH1G):c.*1098T>A rs116670727 0.00377
NM_173477.5(USH1G):c.*776G>A rs55847044 0.00248
NM_173477.5(USH1G):c.*1821C>G rs74943260 0.00056

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