rs7069292
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7069292(C;C) |
| Make rs7069292(C;T) |
| Make rs7069292(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 18258059 |
| Gene | CACNB2, LOC107984213 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7069292 |
| dbSNP (classic) | rs7069292 |
| ClinGen | rs7069292 |
| ebi | rs7069292 |
| HLI | rs7069292 |
| Exac | rs7069292 |
| Gnomad | rs7069292 |
| Varsome | rs7069292 |
| LitVar | rs7069292 |
| Map | rs7069292 |
| PheGenI | rs7069292 |
| Biobank | rs7069292 |
| 1000 genomes | rs7069292 |
| hgdp | rs7069292 |
| ensembl | rs7069292 |
| geneview | rs7069292 |
| scholar | rs7069292 |
| rs7069292 | |
| pharmgkb | rs7069292 |
| gwascentral | rs7069292 |
| openSNP | rs7069292 |
| 23andMe | rs7069292 |
| SNPshot | rs7069292 |
| SNPdbe | rs7069292 |
| MSV3d | rs7069292 |
| GWAS Ctlg | rs7069292 |
| GMAF | 0.1905 |
| Max Magnitude | 0 |
[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 23744328] [Association between CACNB2 gene polymorphisms and essential hypertension]
