rs7789940
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7789940(A;A) |
| Make rs7789940(A;G) |
| Make rs7789940(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 76321913 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7789940 |
| dbSNP (classic) | rs7789940 |
| ClinGen | rs7789940 |
| ebi | rs7789940 |
| HLI | rs7789940 |
| Exac | rs7789940 |
| Gnomad | rs7789940 |
| Varsome | rs7789940 |
| LitVar | rs7789940 |
| Map | rs7789940 |
| PheGenI | rs7789940 |
| Biobank | rs7789940 |
| 1000 genomes | rs7789940 |
| hgdp | rs7789940 |
| ensembl | rs7789940 |
| geneview | rs7789940 |
| scholar | rs7789940 |
| rs7789940 | |
| pharmgkb | rs7789940 |
| gwascentral | rs7789940 |
| openSNP | rs7789940 |
| 23andMe | rs7789940 |
| SNPshot | rs7789940 |
| SNPdbe | rs7789940 |
| MSV3d | rs7789940 |
| GWAS Ctlg | rs7789940 |
| GMAF | 0.3402 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21654844 ]
|
| Trait | |
| Title | Genome-wide association study of severity in multiple sclerosis. |
| Risk Allele | G |
| P-val | 0.000006 |
| Odds Ratio | 1.8700 [NR] |
