rs4684792
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4684792(C;C) |
| Make rs4684792(C;T) |
| Make rs4684792(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 11652993 |
| Gene | VGLL4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4684792 |
| dbSNP (classic) | rs4684792 |
| ClinGen | rs4684792 |
| ebi | rs4684792 |
| HLI | rs4684792 |
| Exac | rs4684792 |
| Gnomad | rs4684792 |
| Varsome | rs4684792 |
| LitVar | rs4684792 |
| Map | rs4684792 |
| PheGenI | rs4684792 |
| Biobank | rs4684792 |
| 1000 genomes | rs4684792 |
| hgdp | rs4684792 |
| ensembl | rs4684792 |
| geneview | rs4684792 |
| scholar | rs4684792 |
| rs4684792 | |
| pharmgkb | rs4684792 |
| gwascentral | rs4684792 |
| openSNP | rs4684792 |
| 23andMe | rs4684792 |
| SNPshot | rs4684792 |
| SNPdbe | rs4684792 |
| MSV3d | rs4684792 |
| GWAS Ctlg | rs4684792 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24068947 ]
|
| Trait | Relative hand skill in reading disability |
| Title | Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. |
| Risk Allele | |
| P-val | 9E-6 |
| Odds Ratio | .28 [0.16-0.4] unit decrease |
