rs1419228
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1419228(A;A) |
| Make rs1419228(A;G) |
| Make rs1419228(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 24178078 |
| Gene | DCDC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1419228 |
| dbSNP (classic) | rs1419228 |
| ClinGen | rs1419228 |
| ebi | rs1419228 |
| HLI | rs1419228 |
| Exac | rs1419228 |
| Gnomad | rs1419228 |
| Varsome | rs1419228 |
| LitVar | rs1419228 |
| Map | rs1419228 |
| PheGenI | rs1419228 |
| Biobank | rs1419228 |
| 1000 genomes | rs1419228 |
| hgdp | rs1419228 |
| ensembl | rs1419228 |
| geneview | rs1419228 |
| scholar | rs1419228 |
| rs1419228 | |
| pharmgkb | rs1419228 |
| gwascentral | rs1419228 |
| openSNP | rs1419228 |
| 23andMe | rs1419228 |
| SNPshot | rs1419228 |
| SNPdbe | rs1419228 |
| MSV3d | rs1419228 |
| GWAS Ctlg | rs1419228 |
| GMAF | 0.2319 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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
[PMID 15717286] Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
[PMID 16385449] Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
