LAMA2, laminin subunit alpha 2, 3908

N. diseases: 167; N. variants: 127
Disease: Refractive Errors ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12205363
rs12205363
Entrez Id: 3908;102723409
Gene Symbol: LAMA2;LOC102723409
LAMA2;LOC102723409
CUI: C0034951
Disease:
Refractive Errors 		C 0.700 GeneticVariation GWASDB Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134 2013