rs10011926
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10011926(C;C) |
| Make rs10011926(C;T) |
| Make rs10011926(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 110105771 |
| Gene | ELOVL6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10011926 |
| dbSNP (classic) | rs10011926 |
| ClinGen | rs10011926 |
| ebi | rs10011926 |
| HLI | rs10011926 |
| Exac | rs10011926 |
| Gnomad | rs10011926 |
| Varsome | rs10011926 |
| LitVar | rs10011926 |
| Map | rs10011926 |
| PheGenI | rs10011926 |
| Biobank | rs10011926 |
| 1000 genomes | rs10011926 |
| hgdp | rs10011926 |
| ensembl | rs10011926 |
| geneview | rs10011926 |
| scholar | rs10011926 |
| rs10011926 | |
| pharmgkb | rs10011926 |
| gwascentral | rs10011926 |
| openSNP | rs10011926 |
| 23andMe | rs10011926 |
| SNPshot | rs10011926 |
| SNPdbe | rs10011926 |
| MSV3d | rs10011926 |
| GWAS Ctlg | rs10011926 |
| GMAF | 0.3802 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20732626 ]
|
| Trait | |
| Title | Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder |
| Risk Allele | |
| P-val | 0.000008 |
| Odds Ratio | 1.49 [NR] |
