rs2602397
From SNPedia
| Merged into | rs1597944 |
| Orientation | plus |
| Stabilized | plus |
| Make rs2602397(C;C) |
| Make rs2602397(C;T) |
| Make rs2602397(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 233595452 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2602397 |
| dbSNP (classic) | rs2602397 |
| ClinGen | rs2602397 |
| ebi | rs2602397 |
| HLI | rs2602397 |
| Exac | rs2602397 |
| Gnomad | rs2602397 |
| Varsome | rs2602397 |
| LitVar | rs2602397 |
| Map | rs2602397 |
| PheGenI | rs2602397 |
| Biobank | rs2602397 |
| 1000 genomes | rs2602397 |
| hgdp | rs2602397 |
| ensembl | rs2602397 |
| geneview | rs2602397 |
| scholar | rs2602397 |
| rs2602397 | |
| pharmgkb | rs2602397 |
| gwascentral | rs2602397 |
| openSNP | rs2602397 |
| 23andMe | rs2602397 |
| SNPshot | rs2602397 |
| SNPdbe | rs2602397 |
| MSV3d | rs2602397 |
| GWAS Ctlg | rs2602397 |
| Status | Merged into rs1597944 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Brain lesion load |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000004 |
| Odds Ratio | NR NR |
