rs1800795(C;G)
Complex; see details
- Magnitude
- 0.0Typical
- Repute
- Not rated
- Frequency
- 17%Average of 10 populations
- On SNPedia
- rs1800795(C;G)
- Gene
- IL6
Frequency
Share of people with C;G in each HapMap population.
- European ancestry (Utah)43%
- Tuscan43%
- Mexican ancestry (Los Angeles)35%
- Gujarati Indian24%
- African ancestry (Southwest US)19%
- Maasai (Kenya)10%
- Chinese (Denver)<1%
- Han Chinese (Beijing)0%
- Japanese (Tokyo)0%
- Yoruba (Nigeria)0%
Other genotypes of rs1800795
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(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.