rs4149579(T;T)
Tumor Necrosis Factor 1A Receptor Intron Variant Homozygous
- Magnitude
- 1.0Minor
- Repute
- Not rated
- Frequency
- <1%Average of 7 populations
- On SNPedia
- rs4149579(A;A)Minus strand
- Gene
- TNFRSF1A
Frequency
Share of people with T;T in each HapMap population.
- European ancestry (Utah)<1%
- Han Chinese (Beijing)0%
- African ancestry (Southwest US)0%
- Chinese (Denver)0%
- Gujarati Indian0%
- Mexican ancestry (Los Angeles)0%
- Tuscan0%
Other genotypes of rs4149579
Notes
From SNPedia
Homozygous for variant SNP in intron of TNF alpha receptor, unknown significance
Source and license
Adapted from rs4149579(A;A) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.