rs7169523
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7169523(A;A) |
| Make rs7169523(A;G) |
| Make rs7169523(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 31171175 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7169523 |
| dbSNP (classic) | rs7169523 |
| ClinGen | rs7169523 |
| ebi | rs7169523 |
| HLI | rs7169523 |
| Exac | rs7169523 |
| Gnomad | rs7169523 |
| Varsome | rs7169523 |
| LitVar | rs7169523 |
| Map | rs7169523 |
| PheGenI | rs7169523 |
| Biobank | rs7169523 |
| 1000 genomes | rs7169523 |
| hgdp | rs7169523 |
| ensembl | rs7169523 |
| geneview | rs7169523 |
| scholar | rs7169523 |
| rs7169523 | |
| pharmgkb | rs7169523 |
| gwascentral | rs7169523 |
| openSNP | rs7169523 |
| 23andMe | rs7169523 |
| SNPshot | rs7169523 |
| SNPdbe | rs7169523 |
| MSV3d | rs7169523 |
| GWAS Ctlg | rs7169523 |
| GMAF | 0.2897 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23055271 ]
|
| Trait | Myasthenia gravis |
| Title | Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. |
| Risk Allele | G |
| P-val | 2E-6 |
| Odds Ratio | 1.40 [1.22-1.60] |
