rs2681492
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs2681492(A;G) |
| Make rs2681492(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 89619312 |
| Gene | ATP2B1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2681492 |
| dbSNP (classic) | rs2681492 |
| ClinGen | rs2681492 |
| ebi | rs2681492 |
| HLI | rs2681492 |
| Exac | rs2681492 |
| Gnomad | rs2681492 |
| Varsome | rs2681492 |
| LitVar | rs2681492 |
| Map | rs2681492 |
| PheGenI | rs2681492 |
| Biobank | rs2681492 |
| 1000 genomes | rs2681492 |
| hgdp | rs2681492 |
| ensembl | rs2681492 |
| geneview | rs2681492 |
| scholar | rs2681492 |
| rs2681492 | |
| pharmgkb | rs2681492 |
| gwascentral | rs2681492 |
| openSNP | rs2681492 |
| 23andMe | rs2681492 |
| SNPshot | rs2681492 |
| SNPdbe | rs2681492 |
| MSV3d | rs2681492 |
| GWAS Ctlg | rs2681492 |
| GMAF | 0.2029 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19430479 ]
|
| Trait | Systolic blood pressure |
| Title | Genome-wide association study of blood pressure and hypertension |
| Risk Allele | T |
| P-val | 4E-11 |
| Odds Ratio | 0.85 [0.60-1.10] mm Hg increase |
[PMID 23036851] Treatment factors rather than genetic variation determine metabolic syndrome in childhood cancer survivors
