rs1567871
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1567871(C;C) |
| Make rs1567871(C;T) |
| Make rs1567871(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 22 |
| Position | 20253637 |
| Gene | LOC105372864, RTN4R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1567871 |
| dbSNP (classic) | rs1567871 |
| ClinGen | rs1567871 |
| ebi | rs1567871 |
| HLI | rs1567871 |
| Exac | rs1567871 |
| Gnomad | rs1567871 |
| Varsome | rs1567871 |
| LitVar | rs1567871 |
| Map | rs1567871 |
| PheGenI | rs1567871 |
| Biobank | rs1567871 |
| 1000 genomes | rs1567871 |
| hgdp | rs1567871 |
| ensembl | rs1567871 |
| geneview | rs1567871 |
| scholar | rs1567871 |
| rs1567871 | |
| pharmgkb | rs1567871 |
| gwascentral | rs1567871 |
| openSNP | rs1567871 |
| 23andMe | rs1567871 |
| SNPshot | rs1567871 |
| SNPdbe | rs1567871 |
| MSV3d | rs1567871 |
| GWAS Ctlg | rs1567871 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26083872] A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population
[PMID 29706887
] The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population.
