rs6850606
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6850606(A;A) |
| Make rs6850606(A;G) |
| Make rs6850606(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 42862679 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6850606 |
| dbSNP (classic) | rs6850606 |
| ClinGen | rs6850606 |
| ebi | rs6850606 |
| HLI | rs6850606 |
| Exac | rs6850606 |
| Gnomad | rs6850606 |
| Varsome | rs6850606 |
| LitVar | rs6850606 |
| Map | rs6850606 |
| PheGenI | rs6850606 |
| Biobank | rs6850606 |
| 1000 genomes | rs6850606 |
| hgdp | rs6850606 |
| ensembl | rs6850606 |
| geneview | rs6850606 |
| scholar | rs6850606 |
| rs6850606 | |
| pharmgkb | rs6850606 |
| gwascentral | rs6850606 |
| openSNP | rs6850606 |
| 23andMe | rs6850606 |
| SNPshot | rs6850606 |
| SNPdbe | rs6850606 |
| MSV3d | rs6850606 |
| GWAS Ctlg | rs6850606 |
| GMAF | 0.421 |
| 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 | A |
| P-val | 3E-6 |
| Odds Ratio | 1.35 [1.19-1.53] |
