rs296547
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs296547(A;A) |
| Make rs296547(A;G) |
| Make rs296547(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 200923009 |
| Gene | MROH3P |
| is a | snp |
| is | mentioned by |
| dbSNP | rs296547 |
| dbSNP (classic) | rs296547 |
| ClinGen | rs296547 |
| ebi | rs296547 |
| HLI | rs296547 |
| Exac | rs296547 |
| Gnomad | rs296547 |
| Varsome | rs296547 |
| LitVar | rs296547 |
| Map | rs296547 |
| PheGenI | rs296547 |
| Biobank | rs296547 |
| 1000 genomes | rs296547 |
| hgdp | rs296547 |
| ensembl | rs296547 |
| geneview | rs296547 |
| scholar | rs296547 |
| rs296547 | |
| pharmgkb | rs296547 |
| gwascentral | rs296547 |
| openSNP | rs296547 |
| 23andMe | rs296547 |
| SNPshot | rs296547 |
| SNPdbe | rs296547 |
| MSV3d | rs296547 |
| GWAS Ctlg | rs296547 |
| GMAF | 0.4945 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752 ]
|
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | |
| P-val | 4E-9 |
| Odds Ratio | 1.12 [1.09-1.16] |
[PMID 21437271] Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases.
[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression
