List of variants in gene USH1G reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_173477.5(USH1G):c.1093G>A (p.Asp365Asn)	rs538983393	0.00001
NM_173477.5(USH1G):c.511G>T (p.Glu171Ter)	rs201866631	0.00001
NM_173477.5(USH1G):c.314C>T (p.Ala105Val)	rs1567940507
NM_173477.5(USH1G):c.812del (p.Pro271fs)	rs1567939793
NM_173477.5(USH1G):c.854dup (p.Ala286fs)	rs1567939718

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