rs2228946
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs2228946(A;A) |
| Make rs2228946(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117278031 |
| Gene | WNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2228946 |
| dbSNP (classic) | rs2228946 |
| ClinGen | rs2228946 |
| ebi | rs2228946 |
| HLI | rs2228946 |
| Exac | rs2228946 |
| Gnomad | rs2228946 |
| Varsome | rs2228946 |
| LitVar | rs2228946 |
| Map | rs2228946 |
| PheGenI | rs2228946 |
| Biobank | rs2228946 |
| 1000 genomes | rs2228946 |
| hgdp | rs2228946 |
| ensembl | rs2228946 |
| geneview | rs2228946 |
| scholar | rs2228946 |
| rs2228946 | |
| pharmgkb | rs2228946 |
| gwascentral | rs2228946 |
| openSNP | rs2228946 |
| 23andMe | rs2228946 |
| SNPshot | rs2228946 |
| SNPdbe | rs2228946 |
| MSV3d | rs2228946 |
| GWAS Ctlg | rs2228946 |
| GMAF | 0.1919 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22522212] The WNT2 gene polymorphism associated with speech delay inherent to autism
[PMID 19838307
] Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes.
