Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3778
Gene Symbol: KCNMA1
KCNMA1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.110 GeneticVariation BEFREE Of the 50 myopia-associated loci, we did not find any variant specifically associated with MMD, but the KCNMA1 and GJD2 loci were significantly associated with HM in highly myopic subjects with MMD, compared to emmetropes. 31415580

2019