rs7119375
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7119375(A;A) |
| Make rs7119375(A;G) |
| Make rs7119375(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 57238490 |
| Gene | APLNR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7119375 |
| dbSNP (classic) | rs7119375 |
| ClinGen | rs7119375 |
| ebi | rs7119375 |
| HLI | rs7119375 |
| Exac | rs7119375 |
| Gnomad | rs7119375 |
| Varsome | rs7119375 |
| LitVar | rs7119375 |
| Map | rs7119375 |
| PheGenI | rs7119375 |
| Biobank | rs7119375 |
| 1000 genomes | rs7119375 |
| hgdp | rs7119375 |
| ensembl | rs7119375 |
| geneview | rs7119375 |
| scholar | rs7119375 |
| rs7119375 | |
| pharmgkb | rs7119375 |
| gwascentral | rs7119375 |
| openSNP | rs7119375 |
| 23andMe | rs7119375 |
| SNPshot | rs7119375 |
| SNPdbe | rs7119375 |
| MSV3d | rs7119375 |
| GWAS Ctlg | rs7119375 |
| GMAF | 0.2259 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[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.
[PMID 33327224] The APLNR gene polymorphism rs7119375 is associated with an increased risk of development of essential hypertension in the Chinese population: A meta-analysis.
