rs514000
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs514000(C;C) |
| Make rs514000(C;T) |
| Make rs514000(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 18 |
| Position | 12854073 |
| Gene | PTPN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs514000 |
| dbSNP (classic) | rs514000 |
| ClinGen | rs514000 |
| ebi | rs514000 |
| HLI | rs514000 |
| Exac | rs514000 |
| Gnomad | rs514000 |
| Varsome | rs514000 |
| LitVar | rs514000 |
| Map | rs514000 |
| PheGenI | rs514000 |
| Biobank | rs514000 |
| 1000 genomes | rs514000 |
| hgdp | rs514000 |
| ensembl | rs514000 |
| geneview | rs514000 |
| scholar | rs514000 |
| rs514000 | |
| pharmgkb | rs514000 |
| gwascentral | rs514000 |
| openSNP | rs514000 |
| 23andMe | rs514000 |
| SNPshot | rs514000 |
| SNPdbe | rs514000 |
| MSV3d | rs514000 |
| GWAS Ctlg | rs514000 |
| Max Magnitude | 0 |
Implicated in a 2015 Korean cohort for Crohn's disease. [PMID: 25489960]
