rs2074225
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2074225(C;C) |
| Make rs2074225(C;T) |
| Make rs2074225(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 61008834 |
| Gene | CD6, LOC105369326 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2074225 |
| dbSNP (classic) | rs2074225 |
| ClinGen | rs2074225 |
| ebi | rs2074225 |
| HLI | rs2074225 |
| Exac | rs2074225 |
| Gnomad | rs2074225 |
| Varsome | rs2074225 |
| LitVar | rs2074225 |
| Map | rs2074225 |
| PheGenI | rs2074225 |
| Biobank | rs2074225 |
| 1000 genomes | rs2074225 |
| hgdp | rs2074225 |
| ensembl | rs2074225 |
| geneview | rs2074225 |
| scholar | rs2074225 |
| rs2074225 | |
| pharmgkb | rs2074225 |
| gwascentral | rs2074225 |
| openSNP | rs2074225 |
| 23andMe | rs2074225 |
| SNPshot | rs2074225 |
| SNPdbe | rs2074225 |
| MSV3d | rs2074225 |
| GWAS Ctlg | rs2074225 |
| GMAF | 0.4559 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23638056
] Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
[PMID 19825846] Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.
