rs11744876
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11744876(A;A) |
| Make rs11744876(A;G) |
| Make rs11744876(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 11084600 |
| Gene | CTNND2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11744876 |
| dbSNP (classic) | rs11744876 |
| ClinGen | rs11744876 |
| ebi | rs11744876 |
| HLI | rs11744876 |
| Exac | rs11744876 |
| Gnomad | rs11744876 |
| Varsome | rs11744876 |
| LitVar | rs11744876 |
| Map | rs11744876 |
| PheGenI | rs11744876 |
| Biobank | rs11744876 |
| 1000 genomes | rs11744876 |
| hgdp | rs11744876 |
| ensembl | rs11744876 |
| geneview | rs11744876 |
| scholar | rs11744876 |
| rs11744876 | |
| pharmgkb | rs11744876 |
| gwascentral | rs11744876 |
| openSNP | rs11744876 |
| 23andMe | rs11744876 |
| SNPshot | rs11744876 |
| SNPdbe | rs11744876 |
| MSV3d | rs11744876 |
| GWAS Ctlg | rs11744876 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 3E-8 |
| Odds Ratio | NR NR |
