rs10883969
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10883969(C;C) |
| Make rs10883969(C;T) |
| Make rs10883969(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 104124358 |
| Gene | SFR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10883969 |
| dbSNP (classic) | rs10883969 |
| ClinGen | rs10883969 |
| ebi | rs10883969 |
| HLI | rs10883969 |
| Exac | rs10883969 |
| Gnomad | rs10883969 |
| Varsome | rs10883969 |
| LitVar | rs10883969 |
| Map | rs10883969 |
| PheGenI | rs10883969 |
| Biobank | rs10883969 |
| 1000 genomes | rs10883969 |
| hgdp | rs10883969 |
| ensembl | rs10883969 |
| geneview | rs10883969 |
| scholar | rs10883969 |
| rs10883969 | |
| pharmgkb | rs10883969 |
| gwascentral | rs10883969 |
| openSNP | rs10883969 |
| 23andMe | rs10883969 |
| SNPshot | rs10883969 |
| SNPdbe | rs10883969 |
| MSV3d | rs10883969 |
| GWAS Ctlg | rs10883969 |
| GMAF | 0.3356 |
| 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 | 2.97 [1.88-4.69] |
