rs996343
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs996343(C;C) |
| Make rs996343(C;T) |
| Make rs996343(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 145321424 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs996343 |
| dbSNP (classic) | rs996343 |
| ClinGen | rs996343 |
| ebi | rs996343 |
| HLI | rs996343 |
| Exac | rs996343 |
| Gnomad | rs996343 |
| Varsome | rs996343 |
| LitVar | rs996343 |
| Map | rs996343 |
| PheGenI | rs996343 |
| Biobank | rs996343 |
| 1000 genomes | rs996343 |
| hgdp | rs996343 |
| ensembl | rs996343 |
| geneview | rs996343 |
| scholar | rs996343 |
| rs996343 | |
| pharmgkb | rs996343 |
| gwascentral | rs996343 |
| openSNP | rs996343 |
| 23andMe | rs996343 |
| SNPshot | rs996343 |
| SNPdbe | rs996343 |
| MSV3d | rs996343 |
| GWAS Ctlg | rs996343 |
| GMAF | 0.4908 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22457343] A genome-wide association study in progressive multiple sclerosis
