rs7679218
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7679218(G;G) |
| Make rs7679218(G;T) |
| Make rs7679218(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 78585710 |
| Gene | ANXA3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7679218 |
| dbSNP (classic) | rs7679218 |
| ClinGen | rs7679218 |
| ebi | rs7679218 |
| HLI | rs7679218 |
| Exac | rs7679218 |
| Gnomad | rs7679218 |
| Varsome | rs7679218 |
| LitVar | rs7679218 |
| Map | rs7679218 |
| PheGenI | rs7679218 |
| Biobank | rs7679218 |
| 1000 genomes | rs7679218 |
| hgdp | rs7679218 |
| ensembl | rs7679218 |
| geneview | rs7679218 |
| scholar | rs7679218 |
| rs7679218 | |
| pharmgkb | rs7679218 |
| gwascentral | rs7679218 |
| openSNP | rs7679218 |
| 23andMe | rs7679218 |
| SNPshot | rs7679218 |
| SNPdbe | rs7679218 |
| MSV3d | rs7679218 |
| GWAS Ctlg | rs7679218 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | 5E-6 |
| Odds Ratio | NR NR |
