rs930876036, SDF4

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
RETINAL CONE DYSTROPHY 1
CUI: C1867326
Disease: RETINAL CONE DYSTROPHY 1
0.010 GeneticVariation BEFREE Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy. 11484154 2001