rs6563695
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6563695(G;G) |
| Make rs6563695(G;T) |
| Make rs6563695(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 39329106 |
| Gene | LOC107984580 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6563695 |
| dbSNP (classic) | rs6563695 |
| ClinGen | rs6563695 |
| ebi | rs6563695 |
| HLI | rs6563695 |
| Exac | rs6563695 |
| Gnomad | rs6563695 |
| Varsome | rs6563695 |
| LitVar | rs6563695 |
| Map | rs6563695 |
| PheGenI | rs6563695 |
| Biobank | rs6563695 |
| 1000 genomes | rs6563695 |
| hgdp | rs6563695 |
| ensembl | rs6563695 |
| geneview | rs6563695 |
| scholar | rs6563695 |
| rs6563695 | |
| pharmgkb | rs6563695 |
| gwascentral | rs6563695 |
| openSNP | rs6563695 |
| 23andMe | rs6563695 |
| SNPshot | rs6563695 |
| SNPdbe | rs6563695 |
| MSV3d | rs6563695 |
| GWAS Ctlg | rs6563695 |
| GMAF | 0.141 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | 5E-6 |
| Odds Ratio | 3.65 [2.09-6.36] |
