rs4363506
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4363506(C;C) |
| Make rs4363506(C;T) |
| Make rs4363506(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 127476239 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4363506 |
| dbSNP (classic) | rs4363506 |
| ClinGen | rs4363506 |
| ebi | rs4363506 |
| HLI | rs4363506 |
| Exac | rs4363506 |
| Gnomad | rs4363506 |
| Varsome | rs4363506 |
| LitVar | rs4363506 |
| Map | rs4363506 |
| PheGenI | rs4363506 |
| Biobank | rs4363506 |
| 1000 genomes | rs4363506 |
| hgdp | rs4363506 |
| ensembl | rs4363506 |
| geneview | rs4363506 |
| scholar | rs4363506 |
| rs4363506 | |
| pharmgkb | rs4363506 |
| gwascentral | rs4363506 |
| openSNP | rs4363506 |
| 23andMe | rs4363506 |
| SNPshot | rs4363506 |
| SNPdbe | rs4363506 |
| MSV3d | rs4363506 |
| GWAS Ctlg | rs4363506 |
| GMAF | 0.4789 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs4363506 |
| PubMedID | [PMID 17362836] |
| Condition | Amyotrophic lateral sclerosis |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 7.00E-007 |
| OR | 1.9 |
| 95% CI | 1.50-2.40 |
[PMID 19740415
] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis
