Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs753942596
rs753942596
PDE6A
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		A 0.710 GeneticVariation CLINVAR

dbSNP: rs753942596
rs753942596
PDE6A
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		A 0.710 CausalMutation CLINVAR