List of variants reported as uncertain significance for perceptual disorders by Institute of Human Genetics, University Hospital Muenster

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.3086G>T (p.Gly1029Val)	rs768158580	0.00002
NM_206933.4(USH2A):c.12299ACA[1] (p.Asn4101del)	rs1657997491

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