rs17787940
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17787940(C;C) |
| Make rs17787940(C;T) |
| Make rs17787940(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 149532802 |
| Gene | WWTR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17787940 |
| dbSNP (classic) | rs17787940 |
| ClinGen | rs17787940 |
| ebi | rs17787940 |
| HLI | rs17787940 |
| Exac | rs17787940 |
| Gnomad | rs17787940 |
| Varsome | rs17787940 |
| LitVar | rs17787940 |
| Map | rs17787940 |
| PheGenI | rs17787940 |
| Biobank | rs17787940 |
| 1000 genomes | rs17787940 |
| hgdp | rs17787940 |
| ensembl | rs17787940 |
| geneview | rs17787940 |
| scholar | rs17787940 |
| rs17787940 | |
| pharmgkb | rs17787940 |
| gwascentral | rs17787940 |
| openSNP | rs17787940 |
| 23andMe | rs17787940 |
| SNPshot | rs17787940 |
| SNPdbe | rs17787940 |
| MSV3d | rs17787940 |
| GWAS Ctlg | rs17787940 |
| GMAF | 0.07025 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23551011 ]
|
| Trait | Preeclampsia |
| Title | Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. |
| Risk Allele | |
| P-val | 3E-6 |
| Odds Ratio | 3.17 [1.95-5.16] |
