rs932764
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs932764(A;A) |
| Make rs932764(A;G) |
| Make rs932764(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94136183 |
| Gene | PLCE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs932764 |
| dbSNP (classic) | rs932764 |
| ClinGen | rs932764 |
| ebi | rs932764 |
| HLI | rs932764 |
| Exac | rs932764 |
| Gnomad | rs932764 |
| Varsome | rs932764 |
| LitVar | rs932764 |
| Map | rs932764 |
| PheGenI | rs932764 |
| Biobank | rs932764 |
| 1000 genomes | rs932764 |
| hgdp | rs932764 |
| ensembl | rs932764 |
| geneview | rs932764 |
| scholar | rs932764 |
| rs932764 | |
| pharmgkb | rs932764 |
| gwascentral | rs932764 |
| openSNP | rs932764 |
| 23andMe | rs932764 |
| SNPshot | rs932764 |
| SNPdbe | rs932764 |
| MSV3d | rs932764 |
| GWAS Ctlg | rs932764 |
| GMAF | 0.4458 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21909115 ]
|
| Trait | |
| Title | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. |
| Risk Allele | G |
| P-val | 8E-7 |
| Odds Ratio | 0.1850 [NR] mmHg increase |
