rs1091047
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1091047(C;C) |
| Make rs1091047(C;G) |
| Make rs1091047(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 24295028 |
| Gene | DCDC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1091047 |
| dbSNP (classic) | rs1091047 |
| ClinGen | rs1091047 |
| ebi | rs1091047 |
| HLI | rs1091047 |
| Exac | rs1091047 |
| Gnomad | rs1091047 |
| Varsome | rs1091047 |
| LitVar | rs1091047 |
| Map | rs1091047 |
| PheGenI | rs1091047 |
| Biobank | rs1091047 |
| 1000 genomes | rs1091047 |
| hgdp | rs1091047 |
| ensembl | rs1091047 |
| geneview | rs1091047 |
| scholar | rs1091047 |
| rs1091047 | |
| pharmgkb | rs1091047 |
| gwascentral | rs1091047 |
| openSNP | rs1091047 |
| 23andMe | rs1091047 |
| SNPshot | rs1091047 |
| SNPdbe | rs1091047 |
| MSV3d | rs1091047 |
| GWAS Ctlg | rs1091047 |
| GMAF | 0.23 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20068590
] Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
