rs10489764
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10489764(C;C) |
| Make rs10489764(C;T) |
| Make rs10489764(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 188116702 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10489764 |
| dbSNP (classic) | rs10489764 |
| ClinGen | rs10489764 |
| ebi | rs10489764 |
| HLI | rs10489764 |
| Exac | rs10489764 |
| Gnomad | rs10489764 |
| Varsome | rs10489764 |
| LitVar | rs10489764 |
| Map | rs10489764 |
| PheGenI | rs10489764 |
| Biobank | rs10489764 |
| 1000 genomes | rs10489764 |
| hgdp | rs10489764 |
| ensembl | rs10489764 |
| geneview | rs10489764 |
| scholar | rs10489764 |
| rs10489764 | |
| pharmgkb | rs10489764 |
| gwascentral | rs10489764 |
| openSNP | rs10489764 |
| 23andMe | rs10489764 |
| SNPshot | rs10489764 |
| SNPdbe | rs10489764 |
| MSV3d | rs10489764 |
| GWAS Ctlg | rs10489764 |
| 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 | 8E-6 |
| Odds Ratio | NR NR |
