"PreventionGenetics, part of Exact Sciences"[submitter] AND "RHO"[gene - ClinVar

	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)	not provided +5 more	GBenign
Select item 13047	NM_000539.3(RHO):c.151G>C (p.Gly51Arg)	RHO (G51R)	Single nucleotide variant (missense variant)	RHO-related disorder +1 more	GPathogenic
Select item 1565902	NM_000539.3(RHO):c.240C>G (p.Ala80=)	RHO	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2183226	NM_000539.3(RHO):c.687C>T (p.Thr229=)	RHO	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 256384	NM_000539.3(RHO):c.696+4C>T	RHO	Single nucleotide variant (intron variant)	not specified +5 more	GBenign
Select item 735910	NM_000539.3(RHO):c.696+9C>T	RHO	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 343282	NM_000539.3(RHO):c.959C>A (p.Thr320Asn)	RHO (T320N)	Single nucleotide variant (missense variant)	Congenital stationary night blindness autosomal dominant 1 +3 more	GConflicting classifications of pathogenicity
Select item 256381	NM_000539.3(RHO):c.*33C>T	RHO	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +2 more	GBenign/Likely benign
Select item 256382	NM_000539.3(RHO):c.*43C>A	RHO	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +5 more	GBenign

ClinVar