rs5050
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs5050(G;G) |
| Make rs5050(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 230714140 |
| Gene | AGT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5050 |
| dbSNP (classic) | rs5050 |
| ClinGen | rs5050 |
| ebi | rs5050 |
| HLI | rs5050 |
| Exac | rs5050 |
| Gnomad | rs5050 |
| Varsome | rs5050 |
| LitVar | rs5050 |
| Map | rs5050 |
| PheGenI | rs5050 |
| Biobank | rs5050 |
| 1000 genomes | rs5050 |
| hgdp | rs5050 |
| ensembl | rs5050 |
| geneview | rs5050 |
| scholar | rs5050 |
| rs5050 | |
| pharmgkb | rs5050 |
| gwascentral | rs5050 |
| openSNP | rs5050 |
| 23andMe | rs5050 |
| SNPshot | rs5050 |
| SNPdbe | rs5050 |
| MSV3d | rs5050 |
| GWAS Ctlg | rs5050 |
| GMAF | 0.174 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21306748
] The association of the angiotensinogen gene with insulin sensitivity in humans: a tagging single nucleotide polymorphism and haplotype approach
[PMID 19105203] An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
[PMID 20808897] Disease-associated mutations that alter the RNA structural ensemble.
[PMID 23716723] The Relationship Between Angiotensinogen Gene Polymorphisms and Essential Hypertension in a Northern Han Chinese Population
[PMID 23648704] Allele-specific expression of angiotensinogen in human subcutaneous adipose tissue.
[PMID 28271690] Genetic Variation in the Renin-Angiotensin System and Diabetic Nephropathy in the Tunisian Population.
[PMID 28361007] Association of angiotensinogen gene SNPs and haplotypes with risk of hypertension in eastern Indian population.
| ClinVar | |
|---|---|
| Risk | rs5050(C;C) rs5050(G;G) |
| Alt | rs5050(C;C) rs5050(G;G) |
| Reference | Rs5050(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Renal dysplasia |
| Variation | info |
| Gene | AGT |
| CLNDBN | Renal dysplasia |
| Reversed | 0 |
| HGVS | NC_000001.10:g.230849886T>G |
| CLNSRC | |
| CLNACC | RCV000377471.1, |
[PMID 32655394] Polymorphisms Involved in Platelet Activation and Inflammatory Response on Aspirin-Related Upper Gastrointestinal Bleeding: A Case-Control Study.
