rs2837960
A SNP in the LINC00323 gene on chromosome 21. Its most notable genotype is G;G: 2.3x rheumatoid arthritis risk
- Gene
- LINC00323
- Location
- Chr 2141,139,991 (GRCh38)
- Highest magnitude
- 2.3Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 21%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G), (G;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.
- AverageG;G 5% G;T 34% T;T 60%
- European ancestry (Utah)G;G 2% G;T 26% T;T 73%
- Han Chinese (Beijing)G;G 5% G;T 29% T;T 66%
- Japanese (Tokyo)G;G <1% G;T 23% T;T 76%
- Yoruba (Nigeria)G;G 10% G;T 45% T;T 46%
- African ancestry (Southwest US)G;G 9% G;T 53% T;T 39%
- Chinese (Denver)G;G 5% G;T 30% T;T 65%
- Gujarati IndianG;G 4% G;T 31% T;T 65%
- Luhya (Kenya)G;G 8% G;T 59% T;T 33%
- Mexican ancestry (Los Angeles)G;G 0% G;T 12% T;T 88%
- Maasai (Kenya)G;G 14% G;T 41% T;T 46%
- TuscanG;G 4% G;T 29% T;T 67%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 120 words
rs2837960 has been reported in a large study to be associated with rheumatoid arthritis. The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 0.95 (CI 0.83-1.08), and for homozygotes, 2.30 (CI 1.64-3.23). Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13. Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis. AntEpiSeeker: detecting epistatic interactions for case-control studies using a two-stage ant colony optimization algorithm.
G;G
The risk allele is (G); the odds ratio associated with homozygotes (G;G) is 2.30 (CI 1.64-3.23). PMID 17554300
References
Source and license
Adapted from rs2837960 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.