rs2070759
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2070759(A;A) |
Make rs2070759(A;C) |
Make rs2070759(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 89623959 |
Gene | ATP2B1 |
is a | snp |
is | mentioned by |
dbSNP | rs2070759 |
dbSNP (classic) | rs2070759 |
ClinGen | rs2070759 |
ebi | rs2070759 |
HLI | rs2070759 |
Exac | rs2070759 |
Gnomad | rs2070759 |
Varsome | rs2070759 |
LitVar | rs2070759 |
Map | rs2070759 |
PheGenI | rs2070759 |
Biobank | rs2070759 |
1000 genomes | rs2070759 |
hgdp | rs2070759 |
ensembl | rs2070759 |
geneview | rs2070759 |
scholar | rs2070759 |
rs2070759 | |
pharmgkb | rs2070759 |
gwascentral | rs2070759 |
openSNP | rs2070759 |
23andMe | rs2070759 |
SNPshot | rs2070759 |
SNPdbe | rs2070759 |
MSV3d | rs2070759 |
GWAS Ctlg | rs2070759 |
GMAF | 0.4862 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 20921432] Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension. The Japanese Millennium Genome Project