rs17149161
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17149161(A;A) |
| Make rs17149161(A;C) |
| Make rs17149161(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 76348912 |
| Gene | YWHAG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17149161 |
| dbSNP (classic) | rs17149161 |
| ClinGen | rs17149161 |
| ebi | rs17149161 |
| HLI | rs17149161 |
| Exac | rs17149161 |
| Gnomad | rs17149161 |
| Varsome | rs17149161 |
| LitVar | rs17149161 |
| Map | rs17149161 |
| PheGenI | rs17149161 |
| Biobank | rs17149161 |
| 1000 genomes | rs17149161 |
| hgdp | rs17149161 |
| ensembl | rs17149161 |
| geneview | rs17149161 |
| scholar | rs17149161 |
| rs17149161 | |
| pharmgkb | rs17149161 |
| gwascentral | rs17149161 |
| openSNP | rs17149161 |
| 23andMe | rs17149161 |
| SNPshot | rs17149161 |
| SNPdbe | rs17149161 |
| MSV3d | rs17149161 |
| GWAS Ctlg | rs17149161 |
| GMAF | 0.3398 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21654844 ]
|
| Trait | |
| Title | Genome-wide association study of severity in multiple sclerosis. |
| Risk Allele | A |
| P-val | 0.000006 |
| Odds Ratio | 1.8700 [NR] |
