rs4374642
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs4374642(C;C) |
| Make rs4374642(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 122179956 |
| Gene | KIAA1109 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4374642 |
| dbSNP (classic) | rs4374642 |
| ClinGen | rs4374642 |
| ebi | rs4374642 |
| HLI | rs4374642 |
| Exac | rs4374642 |
| Gnomad | rs4374642 |
| Varsome | rs4374642 |
| LitVar | rs4374642 |
| Map | rs4374642 |
| PheGenI | rs4374642 |
| Biobank | rs4374642 |
| 1000 genomes | rs4374642 |
| hgdp | rs4374642 |
| ensembl | rs4374642 |
| geneview | rs4374642 |
| scholar | rs4374642 |
| rs4374642 | |
| pharmgkb | rs4374642 |
| gwascentral | rs4374642 |
| openSNP | rs4374642 |
| 23andMe | rs4374642 |
| SNPshot | rs4374642 |
| SNPdbe | rs4374642 |
| MSV3d | rs4374642 |
| GWAS Ctlg | rs4374642 |
| GMAF | 0.1006 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21760890
] Potential celiac patients: a model of celiac disease pathogenesis
[PMID 17558408] A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
