List of variants in gene RHO reported as benign for Retinitis pigmentosa

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000539.3(RHO):c.-26A>G	rs7984	0.38071
NM_000539.3(RHO):c.*912A>G	rs2855558	0.37600
NM_000539.3(RHO):c.*232A>G	rs2410	0.12892
NM_000539.3(RHO):c.*925T>C	rs60645924	0.11065
NM_000539.3(RHO):c.-51G>A	rs2269736	0.08270
NM_000539.3(RHO):c.696+4C>T	rs56340615	0.07633
NM_000539.3(RHO):c.*313C>T	rs55941599	0.02366
NM_000539.3(RHO):c.*1601C>T	rs187923166	0.01177
NM_000539.3(RHO):c.*488T>C	rs78163008	0.01127
NM_000539.3(RHO):c.*33C>T	rs113310993	0.01076
NM_000539.3(RHO):c.*1278G>T	rs113312341	0.00359
NM_000539.3(RHO):c.*1099G>A	rs3733148
NM_000539.3(RHO):c.*43C>A	rs2071093

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