rs7665939
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7665939(C;C) |
| Make rs7665939(C;T) |
| Make rs7665939(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 189202164 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7665939 |
| dbSNP (classic) | rs7665939 |
| ClinGen | rs7665939 |
| ebi | rs7665939 |
| HLI | rs7665939 |
| Exac | rs7665939 |
| Gnomad | rs7665939 |
| Varsome | rs7665939 |
| LitVar | rs7665939 |
| Map | rs7665939 |
| PheGenI | rs7665939 |
| Biobank | rs7665939 |
| 1000 genomes | rs7665939 |
| hgdp | rs7665939 |
| ensembl | rs7665939 |
| geneview | rs7665939 |
| scholar | rs7665939 |
| rs7665939 | |
| pharmgkb | rs7665939 |
| gwascentral | rs7665939 |
| openSNP | rs7665939 |
| 23andMe | rs7665939 |
| SNPshot | rs7665939 |
| SNPdbe | rs7665939 |
| MSV3d | rs7665939 |
| GWAS Ctlg | rs7665939 |
| GMAF | 0.06566 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22959728 ]
|
| Trait | Amyotrophic lateral sclerosis |
| Title | Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. |
| Risk Allele | |
| P-val | 9E-6 |
| Odds Ratio | 1.23 [1.11-1.39] |
