Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61749670
rs61749670
GUCY2D
A 0.700 CausalMutation CLINVAR Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes. 20683928

2010
dbSNP: rs61749670
rs61749670
GUCY2D
A 0.700 CausalMutation CLINVAR Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis. 8944027

1996