rs10087214
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10087214(A;A) |
Make rs10087214(A;G) |
Make rs10087214(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 142918310 |
Gene | CYP11B2 |
is a | snp |
is | mentioned by |
dbSNP | rs10087214 |
dbSNP (classic) | rs10087214 |
ClinGen | rs10087214 |
ebi | rs10087214 |
HLI | rs10087214 |
Exac | rs10087214 |
Gnomad | rs10087214 |
Varsome | rs10087214 |
LitVar | rs10087214 |
Map | rs10087214 |
PheGenI | rs10087214 |
Biobank | rs10087214 |
1000 genomes | rs10087214 |
hgdp | rs10087214 |
ensembl | rs10087214 |
geneview | rs10087214 |
scholar | rs10087214 |
rs10087214 | |
pharmgkb | rs10087214 |
gwascentral | rs10087214 |
openSNP | rs10087214 |
23andMe | rs10087214 |
SNPshot | rs10087214 |
SNPdbe | rs10087214 |
MSV3d | rs10087214 |
GWAS Ctlg | rs10087214 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28953657] A novel haplotype of low-frequency variants in the aldosterone synthase gene among northern Han Chinese with essential hypertension.