rs2685056
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2685056(C;C) |
| Make rs2685056(C;T) |
| Make rs2685056(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 104699729 |
| Gene | LOC107986108 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2685056 |
| dbSNP (classic) | rs2685056 |
| ClinGen | rs2685056 |
| ebi | rs2685056 |
| HLI | rs2685056 |
| Exac | rs2685056 |
| Gnomad | rs2685056 |
| Varsome | rs2685056 |
| LitVar | rs2685056 |
| Map | rs2685056 |
| PheGenI | rs2685056 |
| Biobank | rs2685056 |
| 1000 genomes | rs2685056 |
| hgdp | rs2685056 |
| ensembl | rs2685056 |
| geneview | rs2685056 |
| scholar | rs2685056 |
| rs2685056 | |
| pharmgkb | rs2685056 |
| gwascentral | rs2685056 |
| openSNP | rs2685056 |
| 23andMe | rs2685056 |
| SNPshot | rs2685056 |
| SNPdbe | rs2685056 |
| MSV3d | rs2685056 |
| GWAS Ctlg | rs2685056 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24529757] |
| Trait | Amyotrophic lateral sclerosis (sporadic) |
| Title | A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. |
| Risk Allele | |
| P-val | 4E-8 |
| Odds Ratio | 2.58 [1.939965-3.434586] |
