rs3104767
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3104767(G;G) |
| Make rs3104767(G;T) |
| Make rs3104767(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 52590826 |
| Gene | CASC16 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3104767 |
| dbSNP (classic) | rs3104767 |
| ClinGen | rs3104767 |
| ebi | rs3104767 |
| HLI | rs3104767 |
| Exac | rs3104767 |
| Gnomad | rs3104767 |
| Varsome | rs3104767 |
| LitVar | rs3104767 |
| Map | rs3104767 |
| PheGenI | rs3104767 |
| Biobank | rs3104767 |
| 1000 genomes | rs3104767 |
| hgdp | rs3104767 |
| ensembl | rs3104767 |
| geneview | rs3104767 |
| scholar | rs3104767 |
| rs3104767 | |
| pharmgkb | rs3104767 |
| gwascentral | rs3104767 |
| openSNP | rs3104767 |
| 23andMe | rs3104767 |
| SNPshot | rs3104767 |
| SNPdbe | rs3104767 |
| MSV3d | rs3104767 |
| GWAS Ctlg | rs3104767 |
| GMAF | 0.3949 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21779176 ]
|
| Trait | |
| Title | Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. |
| Risk Allele | G |
| P-val | 9E-19 |
| Odds Ratio | 1.3500 [1.27-1.43] |
[PMID 29404899] TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects.
[PMID 31706190] TOX3 gene variant could be associated with painful restless legs.
