rs2192161
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2192161(C;C) |
| Make rs2192161(C;T) |
| Make rs2192161(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 14309673 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2192161 |
| dbSNP (classic) | rs2192161 |
| ClinGen | rs2192161 |
| ebi | rs2192161 |
| HLI | rs2192161 |
| Exac | rs2192161 |
| Gnomad | rs2192161 |
| Varsome | rs2192161 |
| LitVar | rs2192161 |
| Map | rs2192161 |
| PheGenI | rs2192161 |
| Biobank | rs2192161 |
| 1000 genomes | rs2192161 |
| hgdp | rs2192161 |
| ensembl | rs2192161 |
| geneview | rs2192161 |
| scholar | rs2192161 |
| rs2192161 | |
| pharmgkb | rs2192161 |
| gwascentral | rs2192161 |
| openSNP | rs2192161 |
| 23andMe | rs2192161 |
| SNPshot | rs2192161 |
| SNPdbe | rs2192161 |
| MSV3d | rs2192161 |
| GWAS Ctlg | rs2192161 |
| GMAF | 0.07943 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23738518 ]
|
| Trait | Non-word repetition |
| Title | A genome-wide association study for reading and language abilities in two population cohorts. |
| Risk Allele | A |
| P-val | 7E-8 |
| Odds Ratio | .20 [0.13-0.27] unit increase |
