rs2230201
A SNP in the C3 gene on chromosome 19. Its most notable genotype is C;C: >1.4x risk of lupus
- Gene
- C3
- Location
- Chr 196,713,280 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 22%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2230201 on the minus strand: (A;A), (A;G), (G;G). 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 0% C;T 0% C;C 100%
- European ancestry (Utah)T;T 0% C;T 0% C;C 100%
- Han Chinese (Beijing)T;T 0% C;T 0% C;C 100%
- Japanese (Tokyo)T;T 0% C;T 0% C;C 100%
- Yoruba (Nigeria)T;T 0% C;T 0% C;C 100%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
In ~500 Japanese SLE patients, the (G) allele of rs2230201, a SNP in the C3 gene, is associated with higher risk for systemic lupus erythematosus (SLE). The odds ratio is 1.19 (CI: 1.01-1.41, p=0.038).
Source and license
Adapted from rs2230201 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.