rs61839258
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs61839258(G;G) |
Make rs61839258(G;T) |
Make rs61839258(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 18400709 |
Gene | CACNB2 |
is a | snp |
is | mentioned by |
dbSNP | rs61839258 |
dbSNP (classic) | rs61839258 |
ClinGen | rs61839258 |
ebi | rs61839258 |
HLI | rs61839258 |
Exac | rs61839258 |
Gnomad | rs61839258 |
Varsome | rs61839258 |
LitVar | rs61839258 |
Map | rs61839258 |
PheGenI | rs61839258 |
Biobank | rs61839258 |
1000 genomes | rs61839258 |
hgdp | rs61839258 |
ensembl | rs61839258 |
geneview | rs61839258 |
scholar | rs61839258 |
rs61839258 | |
pharmgkb | rs61839258 |
gwascentral | rs61839258 |
openSNP | rs61839258 |
23andMe | rs61839258 |
SNPshot | rs61839258 |
SNPdbe | rs61839258 |
MSV3d | rs61839258 |
GWAS Ctlg | rs61839258 |
GMAF | 0.169 |
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)