rs4869931
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4869931(A;A) |
| Make rs4869931(A;G) |
| Make rs4869931(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 150688753 |
| Gene | PLEKHG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4869931 |
| dbSNP (classic) | rs4869931 |
| ClinGen | rs4869931 |
| ebi | rs4869931 |
| HLI | rs4869931 |
| Exac | rs4869931 |
| Gnomad | rs4869931 |
| Varsome | rs4869931 |
| LitVar | rs4869931 |
| Map | rs4869931 |
| PheGenI | rs4869931 |
| Biobank | rs4869931 |
| 1000 genomes | rs4869931 |
| hgdp | rs4869931 |
| ensembl | rs4869931 |
| geneview | rs4869931 |
| scholar | rs4869931 |
| rs4869931 | |
| pharmgkb | rs4869931 |
| gwascentral | rs4869931 |
| openSNP | rs4869931 |
| 23andMe | rs4869931 |
| SNPshot | rs4869931 |
| SNPdbe | rs4869931 |
| MSV3d | rs4869931 |
| GWAS Ctlg | rs4869931 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24058526 ]
|
| Trait | Systolic blood pressure in sickle cell anemia |
| Title | Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. |
| Risk Allele | A |
| P-val | 8E-6 |
| Odds Ratio | 1.21 [0.68-1.74] mmHg increase |
