rs1056667
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1056667(C;C) |
| Make rs1056667(C;T) |
| Make rs1056667(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 26510336 |
| Gene | BTN1A1, LOC107986583 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1056667 |
| dbSNP (classic) | rs1056667 |
| ClinGen | rs1056667 |
| ebi | rs1056667 |
| HLI | rs1056667 |
| Exac | rs1056667 |
| Gnomad | rs1056667 |
| Varsome | rs1056667 |
| LitVar | rs1056667 |
| Map | rs1056667 |
| PheGenI | rs1056667 |
| Biobank | rs1056667 |
| 1000 genomes | rs1056667 |
| hgdp | rs1056667 |
| ensembl | rs1056667 |
| geneview | rs1056667 |
| scholar | rs1056667 |
| rs1056667 | |
| pharmgkb | rs1056667 |
| gwascentral | rs1056667 |
| openSNP | rs1056667 |
| 23andMe | rs1056667 |
| SNPshot | rs1056667 |
| SNPdbe | rs1056667 |
| MSV3d | rs1056667 |
| GWAS Ctlg | rs1056667 |
| GMAF | 0.4518 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23722424 ]
|
| Trait | Educational attainment |
| Title | GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. |
| Risk Allele | T |
| P-val | 2E-8 |
| Odds Ratio | .09 [NR] unit increase |
