rs1056629
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1056629(A;A) |
| Make rs1056629(A;G) |
| Make rs1056629(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 82148499 |
| Gene | MPHOSPH6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1056629 |
| dbSNP (classic) | rs1056629 |
| ClinGen | rs1056629 |
| ebi | rs1056629 |
| HLI | rs1056629 |
| Exac | rs1056629 |
| Gnomad | rs1056629 |
| Varsome | rs1056629 |
| LitVar | rs1056629 |
| Map | rs1056629 |
| PheGenI | rs1056629 |
| Biobank | rs1056629 |
| 1000 genomes | rs1056629 |
| hgdp | rs1056629 |
| ensembl | rs1056629 |
| geneview | rs1056629 |
| scholar | rs1056629 |
| rs1056629 | |
| pharmgkb | rs1056629 |
| gwascentral | rs1056629 |
| openSNP | rs1056629 |
| 23andMe | rs1056629 |
| SNPshot | rs1056629 |
| SNPdbe | rs1056629 |
| MSV3d | rs1056629 |
| GWAS Ctlg | rs1056629 |
| GMAF | 0.202 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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
