rs2235306
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2235306(C;C) |
Make rs2235306(C;T) |
Make rs2235306(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 129650121 |
Gene | APLN |
is a | snp |
is | mentioned by |
dbSNP | rs2235306 |
dbSNP (classic) | rs2235306 |
ClinGen | rs2235306 |
ebi | rs2235306 |
HLI | rs2235306 |
Exac | rs2235306 |
Gnomad | rs2235306 |
Varsome | rs2235306 |
LitVar | rs2235306 |
Map | rs2235306 |
PheGenI | rs2235306 |
Biobank | rs2235306 |
1000 genomes | rs2235306 |
hgdp | rs2235306 |
ensembl | rs2235306 |
geneview | rs2235306 |
scholar | rs2235306 |
rs2235306 | |
pharmgkb | rs2235306 |
gwascentral | rs2235306 |
openSNP | rs2235306 |
23andMe | rs2235306 |
SNPshot | rs2235306 |
SNPdbe | rs2235306 |
MSV3d | rs2235306 |
GWAS Ctlg | rs2235306 |
GMAF | 0.234 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20224560] Association of genetic variants in the apelin-APJ system and ACE2 with blood pressure responses to potassium supplementation: the GenSalt study.
[PMID 19567136] Association of apelin genetic variants with type 2 diabetes and related clinical features in Chinese Hans.
[PMID 20125035] Genetic variants in the apelin system and blood pressure responses to dietary sodium interventions: a family-based association study.