Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893779
rs104893779
RHO
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		T 0.720 GeneticVariation CLINVAR Rhodopsin mutations in autosomal dominant retinitis pigmentosa. 8401533

1993