rs1250552
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1250552(C;C) |
| Make rs1250552(C;T) |
| Make rs1250552(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 79298270 |
| Gene | ZMIZ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1250552 |
| dbSNP (classic) | rs1250552 |
| ClinGen | rs1250552 |
| ebi | rs1250552 |
| HLI | rs1250552 |
| Exac | rs1250552 |
| Gnomad | rs1250552 |
| Varsome | rs1250552 |
| LitVar | rs1250552 |
| Map | rs1250552 |
| PheGenI | rs1250552 |
| Biobank | rs1250552 |
| 1000 genomes | rs1250552 |
| hgdp | rs1250552 |
| ensembl | rs1250552 |
| geneview | rs1250552 |
| scholar | rs1250552 |
| rs1250552 | |
| pharmgkb | rs1250552 |
| gwascentral | rs1250552 |
| openSNP | rs1250552 |
| 23andMe | rs1250552 |
| SNPshot | rs1250552 |
| SNPdbe | rs1250552 |
| MSV3d | rs1250552 |
| GWAS Ctlg | rs1250552 |
| GMAF | 0.4197 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752 ]
|
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | |
| P-val | 9E-10 |
| Odds Ratio | 1.12 [1.09-1.16] |
