rs751728
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs751728(A;A) |
| Make rs751728(A;G) |
| Make rs751728(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 33796256 |
| Gene | LEMD2, LOC105375024, MLN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs751728 |
| dbSNP (classic) | rs751728 |
| ClinGen | rs751728 |
| ebi | rs751728 |
| HLI | rs751728 |
| Exac | rs751728 |
| Gnomad | rs751728 |
| Varsome | rs751728 |
| LitVar | rs751728 |
| Map | rs751728 |
| PheGenI | rs751728 |
| Biobank | rs751728 |
| 1000 genomes | rs751728 |
| hgdp | rs751728 |
| ensembl | rs751728 |
| geneview | rs751728 |
| scholar | rs751728 |
| rs751728 | |
| pharmgkb | rs751728 |
| gwascentral | rs751728 |
| openSNP | rs751728 |
| 23andMe | rs751728 |
| SNPshot | rs751728 |
| SNPdbe | rs751728 |
| MSV3d | rs751728 |
| GWAS Ctlg | rs751728 |
| GMAF | 0.438 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23850713] |
| Trait | Crohn's disease |
| Title | Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations. |
| Risk Allele | T |
| P-val | 1E-8 |
| Odds Ratio | 1.32 [1.20-1.45] |
