rs2664517
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2664517(C;C) |
Make rs2664517(C;T) |
Make rs2664517(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 46016464 |
Gene | MMP9 |
is a | snp |
is | mentioned by |
dbSNP | rs2664517 |
dbSNP (classic) | rs2664517 |
ClinGen | rs2664517 |
ebi | rs2664517 |
HLI | rs2664517 |
Exac | rs2664517 |
Gnomad | rs2664517 |
Varsome | rs2664517 |
LitVar | rs2664517 |
Map | rs2664517 |
PheGenI | rs2664517 |
Biobank | rs2664517 |
1000 genomes | rs2664517 |
hgdp | rs2664517 |
ensembl | rs2664517 |
geneview | rs2664517 |
scholar | rs2664517 |
rs2664517 | |
pharmgkb | rs2664517 |
gwascentral | rs2664517 |
openSNP | rs2664517 |
23andMe | rs2664517 |
SNPshot | rs2664517 |
SNPdbe | rs2664517 |
MSV3d | rs2664517 |
GWAS Ctlg | rs2664517 |
Max Magnitude | 0 |
[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