Disease: Abnormality of refraction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7744813
rs7744813
Entrez Id: 56479
Gene Symbol: KCNQ5
KCNQ5
CUI: C4025843
Disease:
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