rs1457092
| Orientation | minus |
| Stabilized | minus |
| Make rs1457092(G;G) |
| Make rs1457092(G;T) |
| Make rs1457092(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 17193427 |
| Gene | MYO9B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1457092 |
| dbSNP (classic) | rs1457092 |
| ClinGen | rs1457092 |
| ebi | rs1457092 |
| HLI | rs1457092 |
| Exac | rs1457092 |
| Gnomad | rs1457092 |
| Varsome | rs1457092 |
| LitVar | rs1457092 |
| Map | rs1457092 |
| PheGenI | rs1457092 |
| Biobank | rs1457092 |
| 1000 genomes | rs1457092 |
| hgdp | rs1457092 |
| ensembl | rs1457092 |
| geneview | rs1457092 |
| scholar | rs1457092 |
| rs1457092 | |
| pharmgkb | rs1457092 |
| gwascentral | rs1457092 |
| openSNP | rs1457092 |
| 23andMe | rs1457092 |
| SNPshot | rs1457092 |
| SNPdbe | rs1457092 |
| MSV3d | rs1457092 |
| GWAS Ctlg | rs1457092 |
| GMAF | 0.4568 |
| Max Magnitude | 0 |
A 2016 meta-analysis including 8 studies (totaling 2272 cases and 5419 controls) found no significant association for this SNP and celiac disease in Caucasian populations.[PMID 27219348]
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20096742] Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability
[PMID 17176439] No evidence of association of the MYO9B polymorphisms with celiac disease in the Spanish population.
[PMID 17584584] MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population.
[PMID 19142207
] MYO9B polymorphisms in multiple sclerosis.
[PMID 20303373] Association analysis of myosin IXB and type 1 diabetes.
[PMID 21515326] Replication of genetic variation in the MYO9B gene in Crohn's disease.
[PMID 23368647] Frequency of MYO9B polymorphisms in celiac patients and controls
[PMID 27556856] MYO9B gene polymorphisms are associated with the risk of inflammatory bowel diseases.
