rs1800629(A;G)
Complex; generally higher risk for certain diseases
- Magnitude
- 2.0Worth knowing
- Repute
- Bad
- Frequency
- 15%Average of 11 populations
- On SNPedia
- rs1800629(A;G)
- Gene
- TNF
Frequency
Share of people with A;G in each HapMap population.
- European ancestry (Utah)31%
- Tuscan19%
- Yoruba (Nigeria)18%
- Luhya (Kenya)17%
- Han Chinese (Beijing)15%
- Maasai (Kenya)15%
- African ancestry (Southwest US)12%
- Mexican ancestry (Los Angeles)12%
- Gujarati Indian9%
- Chinese (Denver)8%
- Japanese (Tokyo)4%
Other genotypes of rs1800629
Related
- Allograft rejectionCondition
- AsthmaCondition
- Chronic obstructive pulmonary diseaseCondition
- Crohn's diseaseCondition
- GlaucomaCondition
- Graves' diseaseCondition
- HyperthyroidismCondition
- Heart diseaseCondition
- LeprosyCondition
- Liver cancerCondition
- LymphomaCondition
- Non-hodgkin lymphomaCondition
- Multiple sclerosisCondition
- PsoriasisCondition
- Rheumatoid arthritisCondition
- SarcoidosisCondition
Source and license
Adapted from rs1800629(A;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.