"Genome-Nilou Lab"[submitter] AND "RHO"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 256383	NM_000539.3(RHO):c.-26A>G	RHO	Single nucleotide variant (5 prime UTR variant)	Pigmentary retinal dystrophy +5 more	GBenign
Select item 256384	NM_000539.3(RHO):c.696+4C>T	RHO	Single nucleotide variant (intron variant)	Congenital stationary night blindness autosomal dominant 1 +5 more	GBenign
Select item 256382	NM_000539.3(RHO):c.*43C>A	RHO	Single nucleotide variant (3 prime UTR variant)	Congenital stationary night blindness autosomal dominant 1 +5 more	GBenign

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