rs3135338
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3135338(A;A) |
| Make rs3135338(A;G) |
| Make rs3135338(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32433440 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3135338 |
| dbSNP (classic) | rs3135338 |
| ClinGen | rs3135338 |
| ebi | rs3135338 |
| HLI | rs3135338 |
| Exac | rs3135338 |
| Gnomad | rs3135338 |
| Varsome | rs3135338 |
| LitVar | rs3135338 |
| Map | rs3135338 |
| PheGenI | rs3135338 |
| Biobank | rs3135338 |
| 1000 genomes | rs3135338 |
| hgdp | rs3135338 |
| ensembl | rs3135338 |
| geneview | rs3135338 |
| scholar | rs3135338 |
| rs3135338 | |
| pharmgkb | rs3135338 |
| gwascentral | rs3135338 |
| openSNP | rs3135338 |
| 23andMe | rs3135338 |
| SNPshot | rs3135338 |
| SNPdbe | rs3135338 |
| MSV3d | rs3135338 |
| GWAS Ctlg | rs3135338 |
| GMAF | 0.3705 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20159113 ]
|
| Trait | Multiple sclerosis |
| Title | Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene |
| Risk Allele | A |
| P-val | 2E-25 |
| Odds Ratio | 3.43 [NR] |
[PMID 19143815] MHC fine mapping of human type 1 diabetes using the T1DGC data.
