rs1229761
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1229761(G;G) |
| Make rs1229761(G;T) |
| Make rs1229761(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114583668 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1229761 |
| dbSNP (classic) | rs1229761 |
| ClinGen | rs1229761 |
| ebi | rs1229761 |
| HLI | rs1229761 |
| Exac | rs1229761 |
| Gnomad | rs1229761 |
| Varsome | rs1229761 |
| LitVar | rs1229761 |
| Map | rs1229761 |
| PheGenI | rs1229761 |
| Biobank | rs1229761 |
| 1000 genomes | rs1229761 |
| hgdp | rs1229761 |
| ensembl | rs1229761 |
| geneview | rs1229761 |
| scholar | rs1229761 |
| rs1229761 | |
| pharmgkb | rs1229761 |
| gwascentral | rs1229761 |
| openSNP | rs1229761 |
| 23andMe | rs1229761 |
| SNPshot | rs1229761 |
| SNPdbe | rs1229761 |
| MSV3d | rs1229761 |
| GWAS Ctlg | rs1229761 |
| GMAF | 0.2043 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22504457] An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples
