rs10439884
From SNPedia
| Orientation | minus |
| Stabilized | plus |
| Make rs10439884(A;A) |
| Make rs10439884(A;G) |
| Make rs10439884(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 21 |
| Position | 10540506 |
| Gene | TPTE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10439884 |
| dbSNP (classic) | rs10439884 |
| ClinGen | rs10439884 |
| ebi | rs10439884 |
| HLI | rs10439884 |
| Exac | rs10439884 |
| Gnomad | rs10439884 |
| Varsome | rs10439884 |
| LitVar | rs10439884 |
| Map | rs10439884 |
| PheGenI | rs10439884 |
| Biobank | rs10439884 |
| 1000 genomes | rs10439884 |
| hgdp | rs10439884 |
| ensembl | rs10439884 |
| geneview | rs10439884 |
| scholar | rs10439884 |
| rs10439884 | |
| pharmgkb | rs10439884 |
| gwascentral | rs10439884 |
| openSNP | rs10439884 |
| 23andMe | rs10439884 |
| SNPshot | rs10439884 |
| SNPdbe | rs10439884 |
| MSV3d | rs10439884 |
| GWAS Ctlg | rs10439884 |
| Max Magnitude | 0 |
| 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 | A |
| P-val | 2E-6 |
| Odds Ratio | NR NR |
