rs121913555, LIM2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CATARACT 19, MULTIPLE TYPES
CUI: C3809004
Disease: CATARACT 19, MULTIPLE TYPES
0.800 GeneticVariation UNIPROT A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family. 11917274 2002
CATARACT 19, MULTIPLE TYPES
CUI: C3809004
Disease: CATARACT 19, MULTIPLE TYPES
0.800 CausalMutation CLINVAR