rs1800795(G;G)
More IL6; certain risks, see details
- Magnitude
- 2.0Worth knowing
- Repute
- Bad
- Frequency
- 78%Average of 10 populations
- On SNPedia
- rs1800795(G;G)
- Gene
- IL6
Frequency
Share of people with G;G in each HapMap population.
- Han Chinese (Beijing)100%
- Japanese (Tokyo)100%
- Yoruba (Nigeria)100%
- Chinese (Denver)99%
- Maasai (Kenya)90%
- African ancestry (Southwest US)81%
- Gujarati Indian75%
- Mexican ancestry (Los Angeles)66%
- Tuscan42%
- European ancestry (Utah)25%
Other genotypes of rs1800795
Notes
From SNPedia
rs1800795 is a SNP in the promoter of the interleukin-6 IL6 gene, affecting the levels made of this important cytokine. In the literature, it is almost universally referred to as the IL6 "-174" polymorphism. It tends to be quite polymorphic in Caucasians, but Asian and African populations are almost monomorphic (for the (G) allele). The rs1800795(G) allele, generally associated with higher levels of IL6, has been associated with increased risk in the following studies: * The rs1800795(G) allele was significantly associated with type-2 diabetes (odds ratio 1.51, CI: 1.11-2.07, p=0.0096) in a study of 700 elderly Caucasians.PMID 15472205 * Following a kidney transplant, patients with rs1800795(G;G) genotypes have a higher risk of new-onset diabetes and higher C-reactive protein levels) compared to the (C;C) genotype. Since this was more pronounced in overweight patients, the authors suggest that diabetes-inducing drug administration should be limited in overweight patients who are rs1800795(G;G) following renal transplantation.PMID 16837641 * The development of bronchiolitis obliterans syndrome (BOS) after lung transplantation is more likely and happens earlier for rs1800795(G) carriers.PMID 12451269 * Among HIV+ men, the lifetime risk of developing Kaposi sarcoma is higher for rs1800795(G;G) homozygotes compared to (C;C) homozygotes.PMID 11001912 * Patients with Hodgkin's lymphoma who are rs1800795(G;G) were less likely to be successfully treated, with odds ratios for failure of 1.75 (CI: 1.04-2.92, p=0.03).PMID 17496310 * A study of 139 elderly males with acute coronary syndrome (ACS) indicated that rs1800795(G;G) genotypes were at 3.89 fold (CI: 1.71-8.86, p=0.001) higher risk of dying within one year of their ACS event than (C;G) or (C;C) genotypes.PMID 16098388 * Although the odds of having a stroke weren't different, among patients (in this case, under 60 years of age) who did have a stroke those with a rs1800795(G;G) genotype had more severe disability after 1 week (odds ratio 3.2, CI: 1.5-6.6, p=0.002).PMID 14512079 * Among Chinese patients with hypertension, the rs1800795(G) allele is more common, and (G;G) genotypes had significantly higher plasma PAI-1 activity than (C;C) genotypes.PMID 15831362 * In 168 Brazilian patients, rs1800795(G) allele frequency was higher in gastric cancer than in patients with chronic gastritis. PMID 17560462 * Although the odds of having Crohn's disease aren't affected, among 153 children with it, those with the rs1800795(G;G) genotype were more growth-retarded at diagnosis than (C;G) or (C;C) genotypes. (G;G) patients also had higher circulating levels of C-reactive protein (CRP).PMID 16150725 * rs1800795(G) carriers don't increase their high-density lipoprotein (HDL) levels after 24 weeks of aerobic exercise as much as rs1800795(C) carriers.PMID 15904871 * The rs1800795(G;G) genotype was more frequent in Australian infants with sudden infant death syndrome (58%) than in control subjects (38%, p=0.02).PMID 17055359 This was not seen in a Norwegian population.PMID 17509454 * Women with endometriosis who are rs1800795(G) carriers appear to be more likely to develop chocolate cysts, and (G) allele carriers may be at slightly higher risk of developing endometriosis.PMID 12517591 * The rs1800795(G) allele is more frequent in women with hyperandrogenism than in controls.PMID 11889177
Related
- Rheumatoid arthritisCondition
- Heart diseaseCondition
- Type-2 diabetesCondition
- StrokeCondition
- ObesityCondition
- Sudden infant death syndromeCondition
- CancerCondition
- PeriodontitisCondition
- Crohn's diseaseCondition
- EndometriosisCondition
- OtitisCondition
- Prostate cancerCondition
- Alzheimer's diseaseCondition
- LongevityCondition
- OsteoarthritisCondition
- Coronary artery diseaseCondition
Source and license
Adapted from rs1800795(G;G) 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.