List of variants in gene combination LOC122152296, USH2A reported as likely pathogenic for Usher syndrome type 2A; Retinitis pigmentosa 39

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.2332G>T (p.Asp778Tyr)	rs142898216	0.00015
NM_206933.4(USH2A):c.2653C>T (p.His885Tyr)	rs746071929	0.00002
NM_206933.4(USH2A):c.2616del (p.Gly873_Val874insTer)	rs1553320451

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