rs1248993
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1248993(A;A) |
| Make rs1248993(A;G) |
| Make rs1248993(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 28738294 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1248993 |
| dbSNP (classic) | rs1248993 |
| ClinGen | rs1248993 |
| ebi | rs1248993 |
| HLI | rs1248993 |
| Exac | rs1248993 |
| Gnomad | rs1248993 |
| Varsome | rs1248993 |
| LitVar | rs1248993 |
| Map | rs1248993 |
| PheGenI | rs1248993 |
| Biobank | rs1248993 |
| 1000 genomes | rs1248993 |
| hgdp | rs1248993 |
| ensembl | rs1248993 |
| geneview | rs1248993 |
| scholar | rs1248993 |
| rs1248993 | |
| pharmgkb | rs1248993 |
| gwascentral | rs1248993 |
| openSNP | rs1248993 |
| 23andMe | rs1248993 |
| SNPshot | rs1248993 |
| SNPdbe | rs1248993 |
| MSV3d | rs1248993 |
| GWAS Ctlg | rs1248993 |
| GMAF | 0.1111 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 6E-6 |
| Odds Ratio | 4.27 [2.28-8.01] |
