rs2274736
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2274736(C;C) |
| Make rs2274736(C;T) |
| Make rs2274736(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 88472308 |
| Gene | PTPN21 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2274736 |
| dbSNP (classic) | rs2274736 |
| ClinGen | rs2274736 |
| ebi | rs2274736 |
| HLI | rs2274736 |
| Exac | rs2274736 |
| Gnomad | rs2274736 |
| Varsome | rs2274736 |
| LitVar | rs2274736 |
| Map | rs2274736 |
| PheGenI | rs2274736 |
| Biobank | rs2274736 |
| 1000 genomes | rs2274736 |
| hgdp | rs2274736 |
| ensembl | rs2274736 |
| geneview | rs2274736 |
| scholar | rs2274736 |
| rs2274736 | |
| pharmgkb | rs2274736 |
| gwascentral | rs2274736 |
| openSNP | rs2274736 |
| 23andMe | rs2274736 |
| SNPshot | rs2274736 |
| SNPdbe | rs2274736 |
| MSV3d | rs2274736 |
| GWAS Ctlg | rs2274736 |
| GMAF | 0.365 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21752600
] Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia
[PMID 16918960] Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease.
