rs10501367
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10501367(C;C) |
Make rs10501367(C;T) |
Make rs10501367(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 57238113 |
Gene | APLNR |
is a | snp |
is | mentioned by |
dbSNP | rs10501367 |
dbSNP (classic) | rs10501367 |
ClinGen | rs10501367 |
ebi | rs10501367 |
HLI | rs10501367 |
Exac | rs10501367 |
Gnomad | rs10501367 |
Varsome | rs10501367 |
LitVar | rs10501367 |
Map | rs10501367 |
PheGenI | rs10501367 |
Biobank | rs10501367 |
1000 genomes | rs10501367 |
hgdp | rs10501367 |
ensembl | rs10501367 |
geneview | rs10501367 |
scholar | rs10501367 |
rs10501367 | |
pharmgkb | rs10501367 |
gwascentral | rs10501367 |
openSNP | rs10501367 |
23andMe | rs10501367 |
SNPshot | rs10501367 |
SNPdbe | rs10501367 |
MSV3d | rs10501367 |
GWAS Ctlg | rs10501367 |
GMAF | 0.2608 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19307984] Family-based analysis of apelin and AGTRL1 gene polymorphisms with hypertension in Han Chinese
[PMID 20125035] Genetic variants in the apelin system and blood pressure responses to dietary sodium interventions: a family-based association study.
[PMID 20485192] Validation of genetic association in apelin-AGTRL1 system with hypertension in a larger Han Chinese population.