Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs538820015
rs538820015
RHO
0.020 GeneticVariation BEFREE Clinical manifestations of patients who are homozygous for the c.124A>G mutation were within the spectrum associated with arRP. 21295282

2011
dbSNP: rs538820015
rs538820015
RHO
0.020 GeneticVariation BEFREE There were no affected subjects with amino acid substitutions in RHO, and there was 1 control subject with a novel substitution (Ala42Thr) who had no symptoms of RP. 17653048

2007