rs1599971
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1599971(C;C) |
| Make rs1599971(C;T) |
| Make rs1599971(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 113834471 |
| Gene | AP4B1-AS1, PTPN22 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1599971 |
| dbSNP (classic) | rs1599971 |
| ClinGen | rs1599971 |
| ebi | rs1599971 |
| HLI | rs1599971 |
| Exac | rs1599971 |
| Gnomad | rs1599971 |
| Varsome | rs1599971 |
| LitVar | rs1599971 |
| Map | rs1599971 |
| PheGenI | rs1599971 |
| Biobank | rs1599971 |
| 1000 genomes | rs1599971 |
| hgdp | rs1599971 |
| ensembl | rs1599971 |
| geneview | rs1599971 |
| scholar | rs1599971 |
| rs1599971 | |
| pharmgkb | rs1599971 |
| gwascentral | rs1599971 |
| openSNP | rs1599971 |
| 23andMe | rs1599971 |
| SNPshot | rs1599971 |
| SNPdbe | rs1599971 |
| MSV3d | rs1599971 |
| GWAS Ctlg | rs1599971 |
| Merged from | Rs2797415 |
| GMAF | 0.337 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[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.
[PMID 20615141] Association of the protein tyrosine phosphatase nonreceptor 22 haplotypes with autoimmune thyroid disease in the Japanese population.
