Rs478582
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs478582 |
| PheGenI | rs478582 |
| nextbio | rs478582 |
| hapmap | rs478582 |
| 1000 genomes | rs478582 |
| hgdp | rs478582 |
| ensembl | rs478582 |
| gopubmed | rs478582 |
| geneview | rs478582 |
| scholar | rs478582 |
| rs478582 | |
| pharmgkb | rs478582 |
| gwascentral | rs478582 |
| openSNP | rs478582 |
| 23andMe | rs478582 |
| 23andMe all | rs478582 |
| SNP Nexus | |
| SNPshot | rs478582 |
| SNPdbe | rs478582 |
| MSV3d | rs478582 |
| Gene | PTPN2 |
| Chromosome | 18 |
| Orientation | plus |
| GMAF | 0.3004 |
| Position | 12835976 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs478582(C;C) |
| Make rs478582(C;T) |
| Make rs478582(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
[PMID 19951419] Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis
[PMID 21246196] A polymorphism in PTPN2 gene is associated with an earlier onset of type 1 diabetes
[PMID 17554260] Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
[PMID 18987646] The expanding genetic overlap between multiple sclerosis and type I diabetes.
[PMID 19073967] Shared and distinct genetic variants in type 1 diabetes and celiac disease.
