rs6922023
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6922023(A;A) |
| Make rs6922023(A;G) |
| Make rs6922023(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 24347889 |
| Gene | DCDC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6922023 |
| dbSNP (classic) | rs6922023 |
| ClinGen | rs6922023 |
| ebi | rs6922023 |
| HLI | rs6922023 |
| Exac | rs6922023 |
| Gnomad | rs6922023 |
| Varsome | rs6922023 |
| LitVar | rs6922023 |
| Map | rs6922023 |
| PheGenI | rs6922023 |
| Biobank | rs6922023 |
| 1000 genomes | rs6922023 |
| hgdp | rs6922023 |
| ensembl | rs6922023 |
| geneview | rs6922023 |
| scholar | rs6922023 |
| rs6922023 | |
| pharmgkb | rs6922023 |
| gwascentral | rs6922023 |
| openSNP | rs6922023 |
| 23andMe | rs6922023 |
| SNPshot | rs6922023 |
| SNPdbe | rs6922023 |
| MSV3d | rs6922023 |
| GWAS Ctlg | rs6922023 |
| GMAF | 0.2635 |
| 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
