rs7571971
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7571971(C;C) |
| Make rs7571971(C;T) |
| Make rs7571971(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 88595833 |
| Gene | EIF2AK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7571971 |
| dbSNP (classic) | rs7571971 |
| ClinGen | rs7571971 |
| ebi | rs7571971 |
| HLI | rs7571971 |
| Exac | rs7571971 |
| Gnomad | rs7571971 |
| Varsome | rs7571971 |
| LitVar | rs7571971 |
| Map | rs7571971 |
| PheGenI | rs7571971 |
| Biobank | rs7571971 |
| 1000 genomes | rs7571971 |
| hgdp | rs7571971 |
| ensembl | rs7571971 |
| geneview | rs7571971 |
| scholar | rs7571971 |
| rs7571971 | |
| pharmgkb | rs7571971 |
| gwascentral | rs7571971 |
| openSNP | rs7571971 |
| 23andMe | rs7571971 |
| SNPshot | rs7571971 |
| SNPdbe | rs7571971 |
| MSV3d | rs7571971 |
| GWAS Ctlg | rs7571971 |
| GMAF | 0.2874 |
| 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 | 4E-13 |
| Odds Ratio | 1.3300 [1.22-1.43] |
[PMID 23116876] An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.
