rs2142991
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common on affy axiom data |
| Make rs2142991(A;G) |
| Make rs2142991(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 42845657 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2142991 |
| dbSNP (classic) | rs2142991 |
| ClinGen | rs2142991 |
| ebi | rs2142991 |
| HLI | rs2142991 |
| Exac | rs2142991 |
| Gnomad | rs2142991 |
| Varsome | rs2142991 |
| LitVar | rs2142991 |
| Map | rs2142991 |
| PheGenI | rs2142991 |
| Biobank | rs2142991 |
| 1000 genomes | rs2142991 |
| hgdp | rs2142991 |
| ensembl | rs2142991 |
| geneview | rs2142991 |
| scholar | rs2142991 |
| rs2142991 | |
| pharmgkb | rs2142991 |
| gwascentral | rs2142991 |
| openSNP | rs2142991 |
| 23andMe | rs2142991 |
| SNPshot | rs2142991 |
| SNPdbe | rs2142991 |
| MSV3d | rs2142991 |
| GWAS Ctlg | rs2142991 |
| GMAF | 0.1414 |
| 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 | 3E-7 |
| Odds Ratio | 1.3000 [1.18-1.44] |
