rs1802908
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1802908(A;A) |
Make rs1802908(A;G) |
Make rs1802908(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 46016424 |
Gene | MMP9 |
is a | snp |
is | mentioned by |
dbSNP | rs1802908 |
dbSNP (classic) | rs1802908 |
ClinGen | rs1802908 |
ebi | rs1802908 |
HLI | rs1802908 |
Exac | rs1802908 |
Gnomad | rs1802908 |
Varsome | rs1802908 |
LitVar | rs1802908 |
Map | rs1802908 |
PheGenI | rs1802908 |
Biobank | rs1802908 |
1000 genomes | rs1802908 |
hgdp | rs1802908 |
ensembl | rs1802908 |
geneview | rs1802908 |
scholar | rs1802908 |
rs1802908 | |
pharmgkb | rs1802908 |
gwascentral | rs1802908 |
openSNP | rs1802908 |
23andMe | rs1802908 |
SNPshot | rs1802908 |
SNPdbe | rs1802908 |
MSV3d | rs1802908 |
GWAS Ctlg | rs1802908 |
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