Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913555
rs121913555
Entrez Id: 3982
Gene Symbol: LIM2
LIM2
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
dbSNP: rs121913555
rs121913555
Entrez Id: 3982
Gene Symbol: LIM2
LIM2
CUI: C3809004
Disease:
CATARACT 19, MULTIPLE TYPES
C 0.800 CausalMutation CLINVAR