rs1310182
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (T;T) | 0 | common/normal |
| Make rs1310182(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 113830881 |
| Gene | AP4B1-AS1, PTPN22 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1310182 |
| dbSNP (classic) | rs1310182 |
| ClinGen | rs1310182 |
| ebi | rs1310182 |
| HLI | rs1310182 |
| Exac | rs1310182 |
| Gnomad | rs1310182 |
| Varsome | rs1310182 |
| LitVar | rs1310182 |
| Map | rs1310182 |
| PheGenI | rs1310182 |
| Biobank | rs1310182 |
| 1000 genomes | rs1310182 |
| hgdp | rs1310182 |
| ensembl | rs1310182 |
| geneview | rs1310182 |
| scholar | rs1310182 |
| rs1310182 | |
| pharmgkb | rs1310182 |
| gwascentral | rs1310182 |
| openSNP | rs1310182 |
| 23andMe | rs1310182 |
| SNPshot | rs1310182 |
| SNPdbe | rs1310182 |
| MSV3d | rs1310182 |
| GWAS Ctlg | rs1310182 |
| GMAF | 0.4614 |
| Max Magnitude | 0 |
[PMID 20510318] Association of PTPN22 Haplotypes with Type 1 Diabetes in the Japanese Population
[PMID 20615141] Association of the Protein Tyrosine Phosphatase Nonreceptor 22 Haplotypes with Autoimmune Thyroid Disease in the Japanese Population
[PMID 16175503
] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
[PMID 17934143] Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.
[PMID 18341666] Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.
[PMID 18466461] Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.
[PMID 18466529] Comparing strategies for evaluation of candidate genes in case-control studies using family data.
[PMID 18466531] Case-control association analysis of rheumatoid arthritis with candidate genes using related cases.
[PMID 18466575] Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis.
[PMID 21193990] A PTPN22 promoter polymorphism -1123G>C is associated with RA pathogenesis in Chinese.
[PMID 22396730] No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations.
[PMID 25073032] Association Between a Gain-of-Function Variant of PTPN22 and Rejection in Liver Transplantation
[PMID 27888068] Associations of single nucleotide polymorphisms of PTPN22 and Ctla4 genes with the risk of allergic rhinitis in a Chinese Han population.
[PMID 30636557] Single Nucleotide Polymorphisms of PTPN22 Gene in Iranian Patients with Ulcerative Colitis.
