rs1488902
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1488902(C;C) |
| Make rs1488902(C;T) |
| Make rs1488902(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 89611857 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1488902 |
| dbSNP (classic) | rs1488902 |
| ClinGen | rs1488902 |
| ebi | rs1488902 |
| HLI | rs1488902 |
| Exac | rs1488902 |
| Gnomad | rs1488902 |
| Varsome | rs1488902 |
| LitVar | rs1488902 |
| Map | rs1488902 |
| PheGenI | rs1488902 |
| Biobank | rs1488902 |
| 1000 genomes | rs1488902 |
| hgdp | rs1488902 |
| ensembl | rs1488902 |
| geneview | rs1488902 |
| scholar | rs1488902 |
| rs1488902 | |
| pharmgkb | rs1488902 |
| gwascentral | rs1488902 |
| openSNP | rs1488902 |
| 23andMe | rs1488902 |
| SNPshot | rs1488902 |
| SNPdbe | rs1488902 |
| MSV3d | rs1488902 |
| GWAS Ctlg | rs1488902 |
| GMAF | 0.3999 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20801717 ]
|
| Trait | |
| Title | Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study |
| Risk Allele | C |
| P-val | 0.000003 |
| Odds Ratio | 1.1450 [NR] |
