rs34517613
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs34517613(C;C) |
| Make rs34517613(C;T) |
| Make rs34517613(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 28283226 |
| Gene | KRT18P55 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34517613 |
| dbSNP (classic) | rs34517613 |
| ClinGen | rs34517613 |
| ebi | rs34517613 |
| HLI | rs34517613 |
| Exac | rs34517613 |
| Gnomad | rs34517613 |
| Varsome | rs34517613 |
| LitVar | rs34517613 |
| Map | rs34517613 |
| PheGenI | rs34517613 |
| Biobank | rs34517613 |
| 1000 genomes | rs34517613 |
| hgdp | rs34517613 |
| ensembl | rs34517613 |
| geneview | rs34517613 |
| scholar | rs34517613 |
| rs34517613 | |
| pharmgkb | rs34517613 |
| gwascentral | rs34517613 |
| openSNP | rs34517613 |
| 23andMe | rs34517613 |
| SNPshot | rs34517613 |
| SNPdbe | rs34517613 |
| MSV3d | rs34517613 |
| GWAS Ctlg | rs34517613 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24256812 ]
|
| Trait | Amyotrophic lateral sclerosis (sporadic) |
| Title | A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. |
| Risk Allele | T |
| P-val | 9E-9 |
| Odds Ratio | 1.20 [1.12-1.29] |
