rs7999075
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7999075(A;A) |
| Make rs7999075(A;C) |
| Make rs7999075(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 13 |
| Position | 22046068 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7999075 |
| dbSNP (classic) | rs7999075 |
| ClinGen | rs7999075 |
| ebi | rs7999075 |
| HLI | rs7999075 |
| Exac | rs7999075 |
| Gnomad | rs7999075 |
| Varsome | rs7999075 |
| LitVar | rs7999075 |
| Map | rs7999075 |
| PheGenI | rs7999075 |
| Biobank | rs7999075 |
| 1000 genomes | rs7999075 |
| hgdp | rs7999075 |
| ensembl | rs7999075 |
| geneview | rs7999075 |
| scholar | rs7999075 |
| rs7999075 | |
| pharmgkb | rs7999075 |
| gwascentral | rs7999075 |
| openSNP | rs7999075 |
| 23andMe | rs7999075 |
| SNPshot | rs7999075 |
| SNPdbe | rs7999075 |
| MSV3d | rs7999075 |
| GWAS Ctlg | rs7999075 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 1E-6 |
| Odds Ratio | NR NR |
