rs3761935
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common/normal |
| Make rs3761935(G;G) |
| Make rs3761935(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 113829906 |
| Gene | AP4B1-AS1, PTPN22 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3761935 |
| dbSNP (classic) | rs3761935 |
| ClinGen | rs3761935 |
| ebi | rs3761935 |
| HLI | rs3761935 |
| Exac | rs3761935 |
| Gnomad | rs3761935 |
| Varsome | rs3761935 |
| LitVar | rs3761935 |
| Map | rs3761935 |
| PheGenI | rs3761935 |
| Biobank | rs3761935 |
| 1000 genomes | rs3761935 |
| hgdp | rs3761935 |
| ensembl | rs3761935 |
| geneview | rs3761935 |
| scholar | rs3761935 |
| rs3761935 | |
| pharmgkb | rs3761935 |
| gwascentral | rs3761935 |
| openSNP | rs3761935 |
| 23andMe | rs3761935 |
| SNPshot | rs3761935 |
| SNPdbe | rs3761935 |
| MSV3d | rs3761935 |
| GWAS Ctlg | rs3761935 |
| GMAF | 0.1589 |
| Max Magnitude | 0 |
[PMID 19503742
] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients. From the abstract: The six SNPs studied in the PTPN22 gene, including rs3761935, showed no significant association with susceptibility to VKH disease.
[PMID 16175503] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
[PMID 19180477] Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.
