rs1788776
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1788776(A;A) |
| Make rs1788776(A;G) |
| Make rs1788776(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 23664073 |
| Gene | ANKRD29 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1788776 |
| dbSNP (classic) | rs1788776 |
| ClinGen | rs1788776 |
| ebi | rs1788776 |
| HLI | rs1788776 |
| Exac | rs1788776 |
| Gnomad | rs1788776 |
| Varsome | rs1788776 |
| LitVar | rs1788776 |
| Map | rs1788776 |
| PheGenI | rs1788776 |
| Biobank | rs1788776 |
| 1000 genomes | rs1788776 |
| hgdp | rs1788776 |
| ensembl | rs1788776 |
| geneview | rs1788776 |
| scholar | rs1788776 |
| rs1788776 | |
| pharmgkb | rs1788776 |
| gwascentral | rs1788776 |
| openSNP | rs1788776 |
| 23andMe | rs1788776 |
| SNPshot | rs1788776 |
| SNPdbe | rs1788776 |
| MSV3d | rs1788776 |
| GWAS Ctlg | rs1788776 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| 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 | A |
| P-val | 8E-6 |
| Odds Ratio | 1.11 [1.06-1.16] |
