rs1032355
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1032355(A;A) |
| Make rs1032355(A;G) |
| Make rs1032355(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 99618739 |
| Gene | MTTP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1032355 |
| dbSNP (classic) | rs1032355 |
| ClinGen | rs1032355 |
| ebi | rs1032355 |
| HLI | rs1032355 |
| Exac | rs1032355 |
| Gnomad | rs1032355 |
| Varsome | rs1032355 |
| LitVar | rs1032355 |
| Map | rs1032355 |
| PheGenI | rs1032355 |
| Biobank | rs1032355 |
| 1000 genomes | rs1032355 |
| hgdp | rs1032355 |
| ensembl | rs1032355 |
| geneview | rs1032355 |
| scholar | rs1032355 |
| rs1032355 | |
| pharmgkb | rs1032355 |
| gwascentral | rs1032355 |
| openSNP | rs1032355 |
| 23andMe | rs1032355 |
| SNPshot | rs1032355 |
| SNPdbe | rs1032355 |
| MSV3d | rs1032355 |
| GWAS Ctlg | rs1032355 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23936387 ]
|
| Trait | Celiac disease |
| Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
| Risk Allele | C |
| P-val | 5E-6 |
| Odds Ratio | NR NR |
