rs1926723
A SNP in the AGT gene on chromosome 1. Its most notable genotype is T;T: common in clinvar
- Gene
- AGT
- Location
- Chr 1230,704,350 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 14%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1926723 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 74%
- European ancestry (Utah)T;T 82%
- Han Chinese (Beijing)T;T 40%
- Japanese (Tokyo)T;T 40%
- Yoruba (Nigeria)T;T 97%
- African ancestry (Southwest US)T;T 88%
- Chinese (Denver)T;T 51%
- Gujarati IndianT;T 83%
- Luhya (Kenya)T;T 82%
- Mexican ancestry (Los Angeles)T;T 76%
- Maasai (Kenya)T;T 94%
- TuscanT;T 86%
Related
Other AGT SNPs
- rs74315283C;TCarrier for a renal tubular dysgenesis mutationImportant
- rs121912702A;GCarrier for a renal tubular dysgenesis mutationImportant
- rs387906578-;ACarrier for a renal tubular dysgenesis mutationImportant
- rs699G;Gincreased risk of hypertensionWorth knowing
- rs4762G;Gnormal riskTypical
- rs5050T;Tcommon in clinvarTypical
- rs5051C;Cnormal riskTypical
- rs7079G;Gcommon in clinvarTypical
Source and license
Adapted from rs1926723 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.