rs6719884
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6719884(A;A) |
| Make rs6719884(A;C) |
| Make rs6719884(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 58809781 |
| Gene | LINC01122 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6719884 |
| dbSNP (classic) | rs6719884 |
| ClinGen | rs6719884 |
| ebi | rs6719884 |
| HLI | rs6719884 |
| Exac | rs6719884 |
| Gnomad | rs6719884 |
| Varsome | rs6719884 |
| LitVar | rs6719884 |
| Map | rs6719884 |
| PheGenI | rs6719884 |
| Biobank | rs6719884 |
| 1000 genomes | rs6719884 |
| hgdp | rs6719884 |
| ensembl | rs6719884 |
| geneview | rs6719884 |
| scholar | rs6719884 |
| rs6719884 | |
| pharmgkb | rs6719884 |
| gwascentral | rs6719884 |
| openSNP | rs6719884 |
| 23andMe | rs6719884 |
| SNPshot | rs6719884 |
| SNPdbe | rs6719884 |
| MSV3d | rs6719884 |
| GWAS Ctlg | rs6719884 |
| GMAF | 0.449 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | A |
| P-val | 3E-6 |
| Odds Ratio | 1.35 [1.19-1.52] |
