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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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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