ClinVar Miner

List of variants in gene RHO reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
Download table as spreadsheet
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.937-23G>A rs2071092 0.05551
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.360C>T (p.Gly120=) rs79765751 0.00312
NM_000539.3(RHO):c.152G>C (p.Gly51Ala) rs149079952 0.00296
NM_000539.3(RHO):c.558G>A (p.Ser186=) rs145549270 0.00203
NM_000539.3(RHO):c.480C>A (p.Thr160=) rs151063543 0.00180
NM_000539.3(RHO):c.*205C>T rs202215179 0.00170
NM_000539.3(RHO):c.*467A>G rs148165044 0.00161
NM_000539.3(RHO):c.381C>G (p.Ser127=) rs146311684 0.00144
NM_000539.3(RHO):c.30C>T (p.Tyr10=) rs138142023 0.00093
NM_000539.3(RHO):c.969C>T (p.Cys323=) rs142771862 0.00075
NM_000539.3(RHO):c.*1200T>C rs538744995 0.00051
NM_000539.3(RHO):c.891C>T (p.Ser297=) rs142285818 0.00041
NM_000539.3(RHO):c.519C>T (p.Ala173=) rs149722668 0.00029
NM_000539.3(RHO):c.310G>A (p.Val104Ile) rs144317206 0.00015
NM_000539.3(RHO):c.1019C>T (p.Thr340Met) rs148748781 0.00014
NM_000539.3(RHO):c.361+10G>A rs372128112 0.00010
NM_000539.3(RHO):c.744G>A (p.Lys248=) rs141185480 0.00010
NM_000539.3(RHO):c.941G>A (p.Arg314Gln) rs753609310 0.00003
NM_000539.3(RHO):c.124G>A (p.Ala42Thr) rs538820015 0.00001
NM_000539.3(RHO):c.520G>A (p.Gly174Ser) rs527236103 0.00001
NM_000539.3(RHO):c.*1099G>A rs3733148
NM_000539.3(RHO):c.*140del rs796098464
NM_000539.3(RHO):c.*43C>A rs2071093
NM_000539.3(RHO):c.*959A>G rs368910470
NM_000539.3(RHO):c.177C>G (p.Leu59=)
NM_000539.3(RHO):c.361+12del rs376995477
NM_000539.3(RHO):c.696+15dup rs749155432
NM_000539.3(RHO):c.869T>A (p.Ile290Asn)
NM_000539.3(RHO):c.895G>T (p.Ala299Ser) rs779665096

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.