Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs29001566
rs29001566
RHO
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		T 0.740 GeneticVariation CLINVAR Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. 2215617

1990
dbSNP: rs29001566
rs29001566
RHO
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		G 0.740 GeneticVariation CLINVAR