rs17636747
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs17636747(C;T) |
| Make rs17636747(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 105261413 |
| Gene | TGFBRAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17636747 |
| dbSNP (classic) | rs17636747 |
| ClinGen | rs17636747 |
| ebi | rs17636747 |
| HLI | rs17636747 |
| Exac | rs17636747 |
| Gnomad | rs17636747 |
| Varsome | rs17636747 |
| LitVar | rs17636747 |
| Map | rs17636747 |
| PheGenI | rs17636747 |
| Biobank | rs17636747 |
| 1000 genomes | rs17636747 |
| hgdp | rs17636747 |
| ensembl | rs17636747 |
| geneview | rs17636747 |
| scholar | rs17636747 |
| rs17636747 | |
| pharmgkb | rs17636747 |
| gwascentral | rs17636747 |
| openSNP | rs17636747 |
| 23andMe | rs17636747 |
| SNPshot | rs17636747 |
| SNPdbe | rs17636747 |
| MSV3d | rs17636747 |
| GWAS Ctlg | rs17636747 |
| GMAF | 0.0124 |
| 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 | 4E-6 |
| Odds Ratio | 8.35 [3.41-20.46] |
