rs11544636
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs11544636(C;T) |
| Make rs11544636(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 24145668 |
| Gene | NRSN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11544636 |
| dbSNP (classic) | rs11544636 |
| ClinGen | rs11544636 |
| ebi | rs11544636 |
| HLI | rs11544636 |
| Exac | rs11544636 |
| Gnomad | rs11544636 |
| Varsome | rs11544636 |
| LitVar | rs11544636 |
| Map | rs11544636 |
| PheGenI | rs11544636 |
| Biobank | rs11544636 |
| 1000 genomes | rs11544636 |
| hgdp | rs11544636 |
| ensembl | rs11544636 |
| geneview | rs11544636 |
| scholar | rs11544636 |
| rs11544636 | |
| pharmgkb | rs11544636 |
| gwascentral | rs11544636 |
| openSNP | rs11544636 |
| 23andMe | rs11544636 |
| SNPshot | rs11544636 |
| SNPdbe | rs11544636 |
| MSV3d | rs11544636 |
| GWAS Ctlg | rs11544636 |
| GMAF | 0.008264 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 16385449
] Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
