rs1411478
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1411478(A;A) |
| Make rs1411478(A;G) |
| Make rs1411478(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 180993146 |
| Gene | STX6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1411478 |
| dbSNP (classic) | rs1411478 |
| ClinGen | rs1411478 |
| ebi | rs1411478 |
| HLI | rs1411478 |
| Exac | rs1411478 |
| Gnomad | rs1411478 |
| Varsome | rs1411478 |
| LitVar | rs1411478 |
| Map | rs1411478 |
| PheGenI | rs1411478 |
| Biobank | rs1411478 |
| 1000 genomes | rs1411478 |
| hgdp | rs1411478 |
| ensembl | rs1411478 |
| geneview | rs1411478 |
| scholar | rs1411478 |
| rs1411478 | |
| pharmgkb | rs1411478 |
| gwascentral | rs1411478 |
| openSNP | rs1411478 |
| 23andMe | rs1411478 |
| SNPshot | rs1411478 |
| SNPdbe | rs1411478 |
| MSV3d | rs1411478 |
| GWAS Ctlg | rs1411478 |
| GMAF | 0.4256 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21685912 ]
|
| Trait | |
| Title | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. |
| Risk Allele | |
| P-val | 4E-11 |
| Odds Ratio | 1.2700 [1.19-1.37] |
[PMID 23415606] STX6 rs1411478 is not associated with increased risk of Parkinson's disease
[PMID 23116876] An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.
