rs11105378
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11105378(C;C) |
Make rs11105378(C;T) |
Make rs11105378(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 89696964 |
Gene | ATP2B1 |
is a | snp |
is | mentioned by |
dbSNP | rs11105378 |
dbSNP (classic) | rs11105378 |
ClinGen | rs11105378 |
ebi | rs11105378 |
HLI | rs11105378 |
Exac | rs11105378 |
Gnomad | rs11105378 |
Varsome | rs11105378 |
LitVar | rs11105378 |
Map | rs11105378 |
PheGenI | rs11105378 |
Biobank | rs11105378 |
1000 genomes | rs11105378 |
hgdp | rs11105378 |
ensembl | rs11105378 |
geneview | rs11105378 |
scholar | rs11105378 |
rs11105378 | |
pharmgkb | rs11105378 |
gwascentral | rs11105378 |
openSNP | rs11105378 |
23andMe | rs11105378 |
SNPshot | rs11105378 |
SNPdbe | rs11105378 |
MSV3d | rs11105378 |
GWAS Ctlg | rs11105378 |
GMAF | 0.185 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20921432] Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension. The Japanese Millennium Genome Project
[PMID 22229515] Polymorphism near the ATP2B1 gene is associated with hypertension risk in East Asians: A meta-analysis involving 15 909 cases and 18 529 controls