rs3093058
A SNP in the CRP gene on chromosome 1. Its most notable genotype is T;T: common in complete genomics
- Gene
- CRP
- Location
- Chr 1159,715,525 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 4%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3093058 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 4 HapMap populations.
- AverageT;T 92%
- European ancestry (Utah)T;T 100%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 68%
Related
Other CRP SNPs
Notes
From SNPedia
Show notes, about 160 words
Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels. Allelic spectrum of the natural variation in CRP. Genetic variation is associated with C-reactive protein levels in the Third National Health and Nutrition Examination Survey. Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: the Cardiovascular Health Study. Genetic determinants of basal C-reactive protein expression in Filipino systemic lupus erythematosus families. Fine-mapping the genetic basis of CRP regulation in African Americans: a Bayesian approach. C-reactive protein, interleukin-6, and prostate cancer risk in men aged 65 years and older. C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery. Gene polymorphisms in association with emerging cardiovascular risk markers in adult women.
Source and license
Adapted from rs3093058 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.