Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12205363
rs12205363
LAMA2 ; LOC102723409
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction 		C 0.700 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013