Have questions? Visit https://www.reddit.com/r/SNPedia

rs2664517

From SNPedia

Orientationplus
Stabilizedplus
Make rs2664517(C;C)
Make rs2664517(C;T)
Make rs2664517(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position46016464
GeneMMP9, TRIM78P
is asnp
is mentioned by
dbSNPrs2664517
ebirs2664517
HLIrs2664517
Exacrs2664517
Varsomers2664517
Maprs2664517
PheGenIrs2664517
hapmaprs2664517
1000 genomesrs2664517
hgdprs2664517
ensemblrs2664517
gopubmedrs2664517
geneviewrs2664517
scholarrs2664517
googlers2664517
pharmgkbrs2664517
gwascentralrs2664517
openSNPrs2664517
23andMers2664517
23andMe allrs2664517
SNP Nexus

SNPshotrs2664517
SNPdbers2664517
MSV3drs2664517
GWAS Ctlgrs2664517
Max Magnitude

[PMID 23257658] A functional polymorphism at miR-491-5p binding site in the 3'-UTR of MMP-9 gene confers increased risk for atherosclerotic cerebral infarction in a Chinese population