rs3093062
A SNP in the CRP gene on chromosome 1. Its most notable genotype is C;C: common in complete genomics
- Gene
- CRP
- Location
- Chr 1159,714,894 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 4%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3093062 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 3 HapMap populations.
- AverageC;C 100%
- European ancestry (Utah)C;C 100%
- Han Chinese (Beijing)C;C 100%
- Japanese (Tokyo)C;C 100%
Related
Other CRP SNPs
Notes
From SNPedia
Notes
functional haplotypes containing rs3091244/rs3093062 contain rs3093061 which is associated with SLE
Source and license
Adapted from rs3093062 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.