rs2476599
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2476599(A;A) |
| Make rs2476599(A;G) |
| Make rs2476599(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 113820837 |
| Gene | AP4B1-AS1, PTPN22 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2476599 |
| dbSNP (classic) | rs2476599 |
| ClinGen | rs2476599 |
| ebi | rs2476599 |
| HLI | rs2476599 |
| Exac | rs2476599 |
| Gnomad | rs2476599 |
| Varsome | rs2476599 |
| LitVar | rs2476599 |
| Map | rs2476599 |
| PheGenI | rs2476599 |
| Biobank | rs2476599 |
| 1000 genomes | rs2476599 |
| hgdp | rs2476599 |
| ensembl | rs2476599 |
| geneview | rs2476599 |
| scholar | rs2476599 |
| rs2476599 | |
| pharmgkb | rs2476599 |
| gwascentral | rs2476599 |
| openSNP | rs2476599 |
| 23andMe | rs2476599 |
| SNPshot | rs2476599 |
| SNPdbe | rs2476599 |
| MSV3d | rs2476599 |
| GWAS Ctlg | rs2476599 |
| GMAF | 0.2938 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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.
