rs2896218
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2896218(A;A) |
| Make rs2896218(A;G) |
| Make rs2896218(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117279924 |
| Gene | WNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2896218 |
| dbSNP (classic) | rs2896218 |
| ClinGen | rs2896218 |
| ebi | rs2896218 |
| HLI | rs2896218 |
| Exac | rs2896218 |
| Gnomad | rs2896218 |
| Varsome | rs2896218 |
| LitVar | rs2896218 |
| Map | rs2896218 |
| PheGenI | rs2896218 |
| Biobank | rs2896218 |
| 1000 genomes | rs2896218 |
| hgdp | rs2896218 |
| ensembl | rs2896218 |
| geneview | rs2896218 |
| scholar | rs2896218 |
| rs2896218 | |
| pharmgkb | rs2896218 |
| gwascentral | rs2896218 |
| openSNP | rs2896218 |
| 23andMe | rs2896218 |
| SNPshot | rs2896218 |
| SNPdbe | rs2896218 |
| MSV3d | rs2896218 |
| GWAS Ctlg | rs2896218 |
| GMAF | 0.3806 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22522212] The WNT2 gene polymorphism associated with speech delay inherent to autism
[PMID 21575668] Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.
