rs4819388
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4819388(C;C) |
| Make rs4819388(C;T) |
| Make rs4819388(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 44227538 |
| Gene | ICOSLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4819388 |
| dbSNP (classic) | rs4819388 |
| ClinGen | rs4819388 |
| ebi | rs4819388 |
| HLI | rs4819388 |
| Exac | rs4819388 |
| Gnomad | rs4819388 |
| Varsome | rs4819388 |
| LitVar | rs4819388 |
| Map | rs4819388 |
| PheGenI | rs4819388 |
| Biobank | rs4819388 |
| 1000 genomes | rs4819388 |
| hgdp | rs4819388 |
| ensembl | rs4819388 |
| geneview | rs4819388 |
| scholar | rs4819388 |
| rs4819388 | |
| pharmgkb | rs4819388 |
| gwascentral | rs4819388 |
| openSNP | rs4819388 |
| 23andMe | rs4819388 |
| SNPshot | rs4819388 |
| SNPdbe | rs4819388 |
| MSV3d | rs4819388 |
| GWAS Ctlg | rs4819388 |
| GMAF | 0.287 |
| 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 | 2E-9 |
| Odds Ratio | 1.14 [1.09-1.19] |
[PMID 23688438] A functional variant at miR-24 binding site in B7-H2 alters susceptibility to gastric cancer in a Chinese Han population
[PMID 22592522] Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients.
[PMID 23543094] Testing for associations between loci and environmental gradients using latent factor mixed models.
