rs7765678
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs7765678(C;C) |
| Make rs7765678(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 24330316 |
| Gene | DCDC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7765678 |
| dbSNP (classic) | rs7765678 |
| ClinGen | rs7765678 |
| ebi | rs7765678 |
| HLI | rs7765678 |
| Exac | rs7765678 |
| Gnomad | rs7765678 |
| Varsome | rs7765678 |
| LitVar | rs7765678 |
| Map | rs7765678 |
| PheGenI | rs7765678 |
| Biobank | rs7765678 |
| 1000 genomes | rs7765678 |
| hgdp | rs7765678 |
| ensembl | rs7765678 |
| geneview | rs7765678 |
| scholar | rs7765678 |
| rs7765678 | |
| pharmgkb | rs7765678 |
| gwascentral | rs7765678 |
| openSNP | rs7765678 |
| 23andMe | rs7765678 |
| SNPshot | rs7765678 |
| SNPdbe | rs7765678 |
| MSV3d | rs7765678 |
| GWAS Ctlg | rs7765678 |
| GMAF | 0.05877 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20068590
] Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
