Gene entry
AGT
angiotensinogen
- Chromosome
- 1
- Cytoband
- 1q42.2
- Variants (rsID)
- 21
AGT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q42.2). Its official name is “angiotensinogen”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs2067853Benignsingle nucleotide variantRenal tubular dysgenesis
- rs4762Benignsingle nucleotide variantRenal tubular dysgenesis
- rs5049Benignsingle nucleotide variantRenal tubular dysgenesis
- rs5051Benignsingle nucleotide variantRenal tubular dysgenesis|Hypertension, essential, susceptibility to|Crohn disease, association with
- rs699Benignsingle nucleotide variantPreeclampsia, susceptibility to|Susceptibility to progression to renal failure in IgA nephropathy|Hypertension, essential, susceptibility to|Renal tubular dysgenesis|Hypertensive disorder
- rs7079Benignsingle nucleotide variantRenal tubular dysgenesis
- rs61731497Likely benignsingle nucleotide variantRenal tubular dysgenesis
- rs74315283Pathogenicsingle nucleotide variantRenal tubular dysgenesis
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.