rs1237682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1237682(C;C) |
| Make rs1237682(C;T) |
| Make rs1237682(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 113821482 |
| Gene | AP4B1-AS1, PTPN22 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1237682 |
| dbSNP (classic) | rs1237682 |
| ClinGen | rs1237682 |
| ebi | rs1237682 |
| HLI | rs1237682 |
| Exac | rs1237682 |
| Gnomad | rs1237682 |
| Varsome | rs1237682 |
| LitVar | rs1237682 |
| Map | rs1237682 |
| PheGenI | rs1237682 |
| Biobank | rs1237682 |
| 1000 genomes | rs1237682 |
| hgdp | rs1237682 |
| ensembl | rs1237682 |
| geneview | rs1237682 |
| scholar | rs1237682 |
| rs1237682 | |
| pharmgkb | rs1237682 |
| gwascentral | rs1237682 |
| openSNP | rs1237682 |
| 23andMe | rs1237682 |
| SNPshot | rs1237682 |
| SNPdbe | rs1237682 |
| MSV3d | rs1237682 |
| GWAS Ctlg | rs1237682 |
| GMAF | 0.2952 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19503742
] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients
