rs4730775
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4730775(C;C) |
| Make rs4730775(C;T) |
| Make rs4730775(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117277064 |
| Gene | WNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4730775 |
| dbSNP (classic) | rs4730775 |
| ClinGen | rs4730775 |
| ebi | rs4730775 |
| HLI | rs4730775 |
| Exac | rs4730775 |
| Gnomad | rs4730775 |
| Varsome | rs4730775 |
| LitVar | rs4730775 |
| Map | rs4730775 |
| PheGenI | rs4730775 |
| Biobank | rs4730775 |
| 1000 genomes | rs4730775 |
| hgdp | rs4730775 |
| ensembl | rs4730775 |
| geneview | rs4730775 |
| scholar | rs4730775 |
| rs4730775 | |
| pharmgkb | rs4730775 |
| gwascentral | rs4730775 |
| openSNP | rs4730775 |
| 23andMe | rs4730775 |
| SNPshot | rs4730775 |
| SNPdbe | rs4730775 |
| MSV3d | rs4730775 |
| GWAS Ctlg | rs4730775 |
| GMAF | 0.3545 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21732829] |
| Trait | |
| Title | Wnt signaling and Dupuytren's disease. |
| Risk Allele | |
| P-val | 3E-8 |
| Odds Ratio | 1.2000 None |
[PMID 20492734
] No association between polymorphisms of WNT2 and schizophrenia in a Korean population.
[PMID 20626912] Association between polymorphisms of arachidonate 12-lipoxygenase (ALOX12) and schizophrenia in a Korean population.
[PMID 22489561] WNT2 Locus Is Involved in Genetic Susceptibility of Peyronie's Disease.
