MMP2, matrix metallopeptidase 2, 4313

N. diseases: 1021; N. variants: 43
Disease: Central retinal vein occlusion ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs774835704
rs774835704
Entrez Id: 4313
Gene Symbol: MMP2
MMP2
CUI: C0154841
Disease:
Central retinal vein occlusion 		0.010 GeneticVariation BEFREE AGTR1 A1166C and Gpla/lla C807T/G873A polymorphisms are likely to be risk factors for CRVO. 31065901 2019