rs1597944
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1597944(C;C) |
| Make rs1597944(C;T) |
| Make rs1597944(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 233595452 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1597944 |
| dbSNP (classic) | rs1597944 |
| ClinGen | rs1597944 |
| ebi | rs1597944 |
| HLI | rs1597944 |
| Exac | rs1597944 |
| Gnomad | rs1597944 |
| Varsome | rs1597944 |
| LitVar | rs1597944 |
| Map | rs1597944 |
| PheGenI | rs1597944 |
| Biobank | rs1597944 |
| 1000 genomes | rs1597944 |
| hgdp | rs1597944 |
| ensembl | rs1597944 |
| geneview | rs1597944 |
| scholar | rs1597944 |
| rs1597944 | |
| pharmgkb | rs1597944 |
| gwascentral | rs1597944 |
| openSNP | rs1597944 |
| 23andMe | rs1597944 |
| SNPshot | rs1597944 |
| SNPdbe | rs1597944 |
| MSV3d | rs1597944 |
| GWAS Ctlg | rs1597944 |
| Merged from | Rs2602397 |
| GMAF | 0.4394 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19010793
] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
