rs12533005
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12533005(C;C) |
| Make rs12533005(C;G) |
| Make rs12533005(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114416000 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12533005 |
| dbSNP (classic) | rs12533005 |
| ClinGen | rs12533005 |
| ebi | rs12533005 |
| HLI | rs12533005 |
| Exac | rs12533005 |
| Gnomad | rs12533005 |
| Varsome | rs12533005 |
| LitVar | rs12533005 |
| Map | rs12533005 |
| PheGenI | rs12533005 |
| Biobank | rs12533005 |
| 1000 genomes | rs12533005 |
| hgdp | rs12533005 |
| ensembl | rs12533005 |
| geneview | rs12533005 |
| scholar | rs12533005 |
| rs12533005 | |
| pharmgkb | rs12533005 |
| gwascentral | rs12533005 |
| openSNP | rs12533005 |
| 23andMe | rs12533005 |
| SNPshot | rs12533005 |
| SNPdbe | rs12533005 |
| MSV3d | rs12533005 |
| GWAS Ctlg | rs12533005 |
| GMAF | 0.4164 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 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
[PMID 21897444
] Imaging genetics of FOXP2 in dyslexia.
