rs5049
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs5049(A;A) |
| Make rs5049(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 230714337 |
| Gene | AGT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5049 |
| dbSNP (classic) | rs5049 |
| ClinGen | rs5049 |
| ebi | rs5049 |
| HLI | rs5049 |
| Exac | rs5049 |
| Gnomad | rs5049 |
| Varsome | rs5049 |
| LitVar | rs5049 |
| Map | rs5049 |
| PheGenI | rs5049 |
| Biobank | rs5049 |
| 1000 genomes | rs5049 |
| hgdp | rs5049 |
| ensembl | rs5049 |
| geneview | rs5049 |
| scholar | rs5049 |
| rs5049 | |
| pharmgkb | rs5049 |
| gwascentral | rs5049 |
| openSNP | rs5049 |
| 23andMe | rs5049 |
| SNPshot | rs5049 |
| SNPdbe | rs5049 |
| MSV3d | rs5049 |
| GWAS Ctlg | rs5049 |
| GMAF | 0.169 |
| Max Magnitude | 0 |
[PMID 22508051] Renin-Angiotensin-aldosterone system gene polymorphisms and coronary artery disease: detection of gene-gene and gene-environment interactions
[PMID 21157371] A pharmacogenetic analysis of determinants of hypertension and blood pressure response to angiotensin-converting enzyme inhibitor therapy in patients with vascular disease and healthy individuals.
[PMID 21859746
] Genetic and BMI risks for predicting blood pressure in three generations of West African Dogon women.
[PMID 24722536] Relationship of renin-angiotensin-aldosterone system polymorphisms and phenotypes to mortality in Chinese coronary atherosclerosis patients
| ClinVar | |
|---|---|
| Risk | rs5049(A;A) |
| Alt | rs5049(A;A) |
| Reference | Rs5049(G;G) |
| Significance | Non-pathogenic |
| Disease | Renal dysplasia |
| Variation | info |
| Gene | AGT |
| CLNDBN | Renal dysplasia |
| Reversed | 1 |
| HGVS | NC_000001.10:g.230850083C>T |
| CLNSRC | |
| CLNACC | RCV000343947.1, |
