rs3789608
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3789608(C;C) |
| Make rs3789608(C;T) |
| Make rs3789608(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 113855166 |
| Gene | AP4B1-AS1, PTPN22 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3789608 |
| dbSNP (classic) | rs3789608 |
| ClinGen | rs3789608 |
| ebi | rs3789608 |
| HLI | rs3789608 |
| Exac | rs3789608 |
| Gnomad | rs3789608 |
| Varsome | rs3789608 |
| LitVar | rs3789608 |
| Map | rs3789608 |
| PheGenI | rs3789608 |
| Biobank | rs3789608 |
| 1000 genomes | rs3789608 |
| hgdp | rs3789608 |
| ensembl | rs3789608 |
| geneview | rs3789608 |
| scholar | rs3789608 |
| rs3789608 | |
| pharmgkb | rs3789608 |
| gwascentral | rs3789608 |
| openSNP | rs3789608 |
| 23andMe | rs3789608 |
| SNPshot | rs3789608 |
| SNPdbe | rs3789608 |
| MSV3d | rs3789608 |
| GWAS Ctlg | rs3789608 |
| GMAF | 0.1593 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19503742
] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients
[PMID 16175503] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
