rs1768208
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1768208(C;C) |
| Make rs1768208(C;T) |
| Make rs1768208(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 39481512 |
| Gene | MOBP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1768208 |
| dbSNP (classic) | rs1768208 |
| ClinGen | rs1768208 |
| ebi | rs1768208 |
| HLI | rs1768208 |
| Exac | rs1768208 |
| Gnomad | rs1768208 |
| Varsome | rs1768208 |
| LitVar | rs1768208 |
| Map | rs1768208 |
| PheGenI | rs1768208 |
| Biobank | rs1768208 |
| 1000 genomes | rs1768208 |
| hgdp | rs1768208 |
| ensembl | rs1768208 |
| geneview | rs1768208 |
| scholar | rs1768208 |
| rs1768208 | |
| pharmgkb | rs1768208 |
| gwascentral | rs1768208 |
| openSNP | rs1768208 |
| 23andMe | rs1768208 |
| SNPshot | rs1768208 |
| SNPdbe | rs1768208 |
| MSV3d | rs1768208 |
| GWAS Ctlg | rs1768208 |
| GMAF | 0.3489 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21685912 ]
|
| Trait | |
| Title | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. |
| Risk Allele | |
| P-val | 5E-17 |
| Odds Ratio | 1.3700 [1.28-1.49] |
[PMID 23116876] An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.
[PMID 26335643] Appoptosin-Mediated Caspase Cleavage of Tau Contributes to Progressive Supranuclear Palsy Pathogenesis
[PMID 27115769] Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci.
