rs11600901
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11600901(A;A) |
| Make rs11600901(A;G) |
| Make rs11600901(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 118161271 |
| Gene | SCN2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11600901 |
| dbSNP (classic) | rs11600901 |
| ClinGen | rs11600901 |
| ebi | rs11600901 |
| HLI | rs11600901 |
| Exac | rs11600901 |
| Gnomad | rs11600901 |
| Varsome | rs11600901 |
| LitVar | rs11600901 |
| Map | rs11600901 |
| PheGenI | rs11600901 |
| Biobank | rs11600901 |
| 1000 genomes | rs11600901 |
| hgdp | rs11600901 |
| ensembl | rs11600901 |
| geneview | rs11600901 |
| scholar | rs11600901 |
| rs11600901 | |
| pharmgkb | rs11600901 |
| gwascentral | rs11600901 |
| openSNP | rs11600901 |
| 23andMe | rs11600901 |
| SNPshot | rs11600901 |
| SNPdbe | rs11600901 |
| MSV3d | rs11600901 |
| GWAS Ctlg | rs11600901 |
| GMAF | 0.05739 |
| 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 | 9E-6 |
| Odds Ratio | 9.83 [3.58-27.00] |
