rs701428
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs701428(A;A) |
| Make rs701428(A;G) |
| Make rs701428(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 20241019 |
| Gene | RTN4R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs701428 |
| dbSNP (classic) | rs701428 |
| ClinGen | rs701428 |
| ebi | rs701428 |
| HLI | rs701428 |
| Exac | rs701428 |
| Gnomad | rs701428 |
| Varsome | rs701428 |
| LitVar | rs701428 |
| Map | rs701428 |
| PheGenI | rs701428 |
| Biobank | rs701428 |
| 1000 genomes | rs701428 |
| hgdp | rs701428 |
| ensembl | rs701428 |
| geneview | rs701428 |
| scholar | rs701428 |
| rs701428 | |
| pharmgkb | rs701428 |
| gwascentral | rs701428 |
| openSNP | rs701428 |
| 23andMe | rs701428 |
| SNPshot | rs701428 |
| SNPdbe | rs701428 |
| MSV3d | rs701428 |
| GWAS Ctlg | rs701428 |
| GMAF | 0.4688 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24321711
] White matter abnormalities in 22q11.2 deletion syndrome: Preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis
[PMID 19052207] Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.
| GWAS snp | |
|---|---|
| PMID | [PMID 23251661]
|
| Trait | Obesity-related traits |
| Title | Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. |
| Risk Allele | G |
| P-val | 2E-6 |
| Odds Ratio | .04 [NR] pg/mL increase |
[PMID 28139055] Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.
