rs104893781, RHO

N. diseases: 3
Disease: Retinitis Pigmentosa ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Retinitis Pigmentosa
CUI: C0035334
Disease: Retinitis Pigmentosa
0.710 GeneticVariation BEFREE Our results suggest that the Pro-267-Leu rhodopsin mutation is associated with a very mild phenotype of retinitis pigmentosa. 9228242 1997
Retinitis Pigmentosa
CUI: C0035334
Disease: Retinitis Pigmentosa
0.710 GeneticVariation CLINVAR