Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28730814
rs28730814
MMP2
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 GeneticVariation BEFREE The c.1810G>A mutation (p. Arg500His) was detected in three of the 200 patients with high myopia but not in the controls. 23378725

2013