rs5050
A SNP in the AGT gene on chromosome 1. Its most notable genotype is T;T: common in clinvar
- Gene
- AGT
- Location
- Chr 1230,714,140 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 17%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageT;T 71%
- European ancestry (Utah)T;T 76%
- Han Chinese (Beijing)T;T 82%
- Japanese (Tokyo)T;T 58%
- Yoruba (Nigeria)T;T 76%
- African ancestry (Southwest US)T;T 84%
- Chinese (Denver)T;T 71%
- Gujarati IndianT;T 58%
- Luhya (Kenya)T;T 66%
- TuscanT;T 67%
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
- rs5051C;Cnormal riskTypical
- rs7079G;Gcommon in clinvarTypical
- rs1926723T;Tcommon in clinvarTypical
Notes
From SNPedia
Notes
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. Disease-associated mutations that alter the RNA structural ensemble.
Source and license
Adapted from rs5050 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.