rs7079
A SNP in the AGT gene on chromosome 1. Its most notable genotype is G;G: common in clinvar
- Gene
- AGT
- Location
- Chr 1230,702,585 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 20%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs7079 on the minus strand: (C;C). 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.
- AverageG;G 70%
- European ancestry (Utah)G;G 47%
- Han Chinese (Beijing)G;G 72%
- Japanese (Tokyo)G;G 78%
- Yoruba (Nigeria)G;G 88%
- African ancestry (Southwest US)G;G 81%
- Chinese (Denver)G;G 69%
- Gujarati IndianG;G 56%
- Luhya (Kenya)G;G 83%
- Mexican ancestry (Los Angeles)G;G 72%
- Maasai (Kenya)G;G 78%
- TuscanG;G 44%
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
- rs1926723T;Tcommon in clinvarTypical
Source and license
Adapted from rs7079 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.