Annotation Detail
Information
- Associated Genes
- MMP2
- Associated Variants
-
rs11568818
rs2285053 ( ENST00000570308.5 )
MMP9 p.Gln279Arg (p.Q279R) ( ENST00000372330.3 )
MMP9 p.Arg574Pro (p.R574P) ( ENST00000372330.3 )
MMP9 p.Arg574Leu (p.R574L) ( ENST00000372330.3 )
MMP9 p.Arg668Gln (p.R668Q) ( ENST00000372330.3 )
MMP9 p.Arg668Pro (p.R668P) ( ENST00000372330.3 )
rs11568818
rs2285053 ( ENST00000570308.5 )
MMP9 p.Gln279Arg (p.Q279R) ( ENST00000372330.3 )
MMP9 p.Arg574Pro (p.R574P) ( ENST00000372330.3 )
MMP9 p.Arg574Leu (p.R574L) ( ENST00000372330.3 )
MMP9 p.Arg668Gln (p.R668Q) ( ENST00000372330.3 )
MMP9 p.Arg668Pro (p.R668P) ( ENST00000372330.3 ) - Associated Disease
- coronary artery disease
- Source Database
- DisGeNET
- Description
- We explored the association of MMP2 (C-735T, rs2285053), MMP7 (A-181G, rs11568818) and MMP9 (R279Q, rs17576), (P574R, rs2250889), (R668Q, rs17577) genetic variants with LVD in coronary artery disease (CAD) patients.
- Pubmed
- 22664146
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.0114540974107551
- Year of publication
- 2012
Drugs