rs9976946
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs9976946(C;C) |
| Make rs9976946(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 34835765 |
| Gene | LOC102724584, RUNX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9976946 |
| dbSNP (classic) | rs9976946 |
| ClinGen | rs9976946 |
| ebi | rs9976946 |
| HLI | rs9976946 |
| Exac | rs9976946 |
| Gnomad | rs9976946 |
| Varsome | rs9976946 |
| LitVar | rs9976946 |
| Map | rs9976946 |
| PheGenI | rs9976946 |
| Biobank | rs9976946 |
| 1000 genomes | rs9976946 |
| hgdp | rs9976946 |
| ensembl | rs9976946 |
| geneview | rs9976946 |
| scholar | rs9976946 |
| rs9976946 | |
| pharmgkb | rs9976946 |
| gwascentral | rs9976946 |
| openSNP | rs9976946 |
| 23andMe | rs9976946 |
| SNPshot | rs9976946 |
| SNPdbe | rs9976946 |
| MSV3d | rs9976946 |
| GWAS Ctlg | rs9976946 |
| GMAF | 0.007346 |
| 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 | 5E-6 |
| Odds Ratio | 5.50 [2.65-11.39] |
