rs5182

A SNP in the AGTR1 gene on chromosome 3. Its most notable genotype is C;C: common in clinvar

Gene
AGTR1
Location
Chr 3148,741,608 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
47%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.032% of people

On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageC;C 32%
  • European ancestry (Utah)C;C 25%
  • Han Chinese (Beijing)C;C 22%
  • Japanese (Tokyo)C;C 9%
  • Yoruba (Nigeria)C;C 71%

Conditions, medicines and genes

Other AGTR1 SNPs

All AGTR1 SNPs

Notes

From SNPedia

Notes

rs5182 (573C/T) is a SNP within the AGTR1 (Angiotensin II receptor type 1). among 4,096 hypertensive subjects, the CT/CC genotypes were associated with reduced risk of heart attack among those treated with ACE inhibitors

Source and license

Adapted from rs5182 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.