rs3816587
A SNP in the ANAPC4 gene on chromosome 4. Its most notable genotype is C;C: 1.3x risk
- Gene
- ANAPC4
- Location
- Chr 425,415,622 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageC;C 34% C;T 47% T;T 19%
- European ancestry (Utah)C;C 18% C;T 49% T;T 33%
- Han Chinese (Beijing)C;C 46% C;T 47% T;T 7%
- Japanese (Tokyo)C;C 45% C;T 43% T;T 12%
- Yoruba (Nigeria)C;C 31% C;T 49% T;T 20%
- African ancestry (Southwest US)C;C 39% C;T 39% T;T 23%
- Chinese (Denver)C;C 51% C;T 39% T;T 10%
- Gujarati IndianC;C 34% C;T 51% T;T 15%
- Luhya (Kenya)C;C 37% C;T 51% T;T 12%
- Mexican ancestry (Los Angeles)C;C 18% C;T 53% T;T 30%
- Maasai (Kenya)C;C 28% C;T 50% T;T 23%
- TuscanC;C 28% C;T 46% T;T 27%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs3816587 has been reported in a large study to be associated with rheumatoid arthritis. The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 0.91 (CI 0.80-1.04), and for homozygotes, 1.35 (CI 1.14-1.59).
Source and license
Adapted from rs3816587 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.