rs6852535
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6852535(A;A) |
| Make rs6852535(A;G) |
| Make rs6852535(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 122557561 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6852535 |
| dbSNP (classic) | rs6852535 |
| ClinGen | rs6852535 |
| ebi | rs6852535 |
| HLI | rs6852535 |
| Exac | rs6852535 |
| Gnomad | rs6852535 |
| Varsome | rs6852535 |
| LitVar | rs6852535 |
| Map | rs6852535 |
| PheGenI | rs6852535 |
| Biobank | rs6852535 |
| 1000 genomes | rs6852535 |
| hgdp | rs6852535 |
| ensembl | rs6852535 |
| geneview | rs6852535 |
| scholar | rs6852535 |
| rs6852535 | |
| pharmgkb | rs6852535 |
| gwascentral | rs6852535 |
| openSNP | rs6852535 |
| 23andMe | rs6852535 |
| SNPshot | rs6852535 |
| SNPdbe | rs6852535 |
| MSV3d | rs6852535 |
| GWAS Ctlg | rs6852535 |
| GMAF | 0.247 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21685912 ]
|
| Trait | |
| Title | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. |
| Risk Allele | |
| P-val | 1E-7 |
| Odds Ratio | 1.2300 [1.13-1.32] |
[PMID 17558408] A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
[PMID 25037274] Autoimmune diseases association study with the KIAA1109-IL2-IL21 region in a Tunisian population
