Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893781
rs104893781
RHO
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
dbSNP: rs104893781
rs104893781
RHO
T 0.710 GeneticVariation CLINVAR