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 |
|---|---|---|
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[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.
