rs11014166
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11014166(A;A) |
| Make rs11014166(A;T) |
| Make rs11014166(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 18419869 |
| Gene | CACNB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11014166 |
| dbSNP (classic) | rs11014166 |
| ClinGen | rs11014166 |
| ebi | rs11014166 |
| HLI | rs11014166 |
| Exac | rs11014166 |
| Gnomad | rs11014166 |
| Varsome | rs11014166 |
| LitVar | rs11014166 |
| Map | rs11014166 |
| PheGenI | rs11014166 |
| Biobank | rs11014166 |
| 1000 genomes | rs11014166 |
| hgdp | rs11014166 |
| ensembl | rs11014166 |
| geneview | rs11014166 |
| scholar | rs11014166 |
| rs11014166 | |
| pharmgkb | rs11014166 |
| gwascentral | rs11014166 |
| openSNP | rs11014166 |
| 23andMe | rs11014166 |
| SNPshot | rs11014166 |
| SNPdbe | rs11014166 |
| MSV3d | rs11014166 |
| GWAS Ctlg | rs11014166 |
| GMAF | 0.2034 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19430479 ]
|
| Trait | Diastolic Blood Pressure |
| Title | Genome-wide association study of blood pressure and hypertension |
| Risk Allele | A |
| P-val | 1E-8 |
| Odds Ratio | 0.37 [0.25-0.49] mm Hg increase |
[PMID 21156931] Genetic Variation in the {beta}2 Subunit of the Voltage-Gated Calcium Channel and Pharmacogenetic Association With Adverse Cardiovascular Outcomes in the INternational VErapamil SR-Trandolapril STudy GENEtic Substudy (INVEST-GENES)
[PMID 21963141] Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in she ethnic minority of China
[PMID 23744328] [Association between CACNB2 gene polymorphisms and essential hypertension]
