C1848634[trait identifier] AND "Molecular Genetics, Royal Melbourne Ho - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1225305	NM_206933.4(USH2A):c.12067-31del	USH2A	Deletion (intron variant)	not provided +2 more	GBenign
Select item 941952	NM_206933.4(USH2A):c.10834G>A (p.Val3612Ile)	USH2A (V3612I)	Single nucleotide variant (missense variant)	Usher syndrome type 2 +4 more	GUncertain significance
Select item 1043673	NM_206933.4(USH2A):c.7787A>G (p.Tyr2596Cys)	USH2A (Y2596C)	Single nucleotide variant (missense variant)	Usher syndrome type 2 +5 more	GUncertain significance

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