rs2357928
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2357928(A;A) |
| Make rs2357928(A;G) |
| Make rs2357928(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 18260712 |
| Gene | CACNB2, LOC107984213 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2357928 |
| dbSNP (classic) | rs2357928 |
| ClinGen | rs2357928 |
| ebi | rs2357928 |
| HLI | rs2357928 |
| Exac | rs2357928 |
| Gnomad | rs2357928 |
| Varsome | rs2357928 |
| LitVar | rs2357928 |
| Map | rs2357928 |
| PheGenI | rs2357928 |
| Biobank | rs2357928 |
| 1000 genomes | rs2357928 |
| hgdp | rs2357928 |
| ensembl | rs2357928 |
| geneview | rs2357928 |
| scholar | rs2357928 |
| rs2357928 | |
| pharmgkb | rs2357928 |
| gwascentral | rs2357928 |
| openSNP | rs2357928 |
| 23andMe | rs2357928 |
| SNPshot | rs2357928 |
| SNPdbe | rs2357928 |
| MSV3d | rs2357928 |
| GWAS Ctlg | rs2357928 |
| GMAF | 0.3792 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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]
