rs2235356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2235356(A;A) |
| Make rs2235356(A;G) |
| Make rs2235356(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 50271920 |
| Gene | MAPK11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2235356 |
| dbSNP (classic) | rs2235356 |
| ClinGen | rs2235356 |
| ebi | rs2235356 |
| HLI | rs2235356 |
| Exac | rs2235356 |
| Gnomad | rs2235356 |
| Varsome | rs2235356 |
| LitVar | rs2235356 |
| Map | rs2235356 |
| PheGenI | rs2235356 |
| Biobank | rs2235356 |
| 1000 genomes | rs2235356 |
| hgdp | rs2235356 |
| ensembl | rs2235356 |
| geneview | rs2235356 |
| scholar | rs2235356 |
| rs2235356 | |
| pharmgkb | rs2235356 |
| gwascentral | rs2235356 |
| openSNP | rs2235356 |
| 23andMe | rs2235356 |
| SNPshot | rs2235356 |
| SNPdbe | rs2235356 |
| MSV3d | rs2235356 |
| GWAS Ctlg | rs2235356 |
| GMAF | 0.4151 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23946768
] A genetic variation of the p38β promoter region is correlated with an increased risk of sporadic colorectal cancer
