rs4789939
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs4789939(A;A) |
| Make rs4789939(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 78885621 |
| Gene | TIMP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4789939 |
| dbSNP (classic) | rs4789939 |
| ClinGen | rs4789939 |
| ebi | rs4789939 |
| HLI | rs4789939 |
| Exac | rs4789939 |
| Gnomad | rs4789939 |
| Varsome | rs4789939 |
| LitVar | rs4789939 |
| Map | rs4789939 |
| PheGenI | rs4789939 |
| Biobank | rs4789939 |
| 1000 genomes | rs4789939 |
| hgdp | rs4789939 |
| ensembl | rs4789939 |
| geneview | rs4789939 |
| scholar | rs4789939 |
| rs4789939 | |
| pharmgkb | rs4789939 |
| gwascentral | rs4789939 |
| openSNP | rs4789939 |
| 23andMe | rs4789939 |
| SNPshot | rs4789939 |
| SNPdbe | rs4789939 |
| MSV3d | rs4789939 |
| GWAS Ctlg | rs4789939 |
| GMAF | 0.3053 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21732829] |
| Trait | |
| Title | Wnt signaling and Dupuytren's disease. |
| Risk Allele | |
| P-val | 6E-7 |
| Odds Ratio | 1.2200 None |
