rs104893768, RHO

N. diseases: 11
Disease: Refractive Errors ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
0.010 GeneticVariation BEFREE The dark-adaptation thresholds, equivalent visual field diameters, and electroretinogram amplitudes (all corrected for age and refractive error) indicated that the disease caused by the NRL mutations was more severe than that caused by the dominant rhodopsin mutation Pro23His and was similar in severity to that produced by the rhodopsin mutation Pro347Leu. 11879142 2002