rs3093664
A SNP in the TNF gene on chromosome 6. Its most notable genotype is A;A: common in complete genomics
- Gene
- TNF
- Location
- Chr 631,576,865 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 7%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other TNF SNPs
- rs3093726C;CProbably an HLA-B*5701 homozygote; high risk for hypersensitivity to various drugs including abacavirVery important
- rs1800629A;Acomplex; generally higher risk for certain diseasesWorth knowing
- rs361525A;Acomplex; generally higher risk for certain diseasesTypical
- rs1800750A;Ahigher acute otitis riskTypical
- rs3093662A;Acommon in complete genomicsTypical
- rs3093665A;Acommon in complete genomicsTypical
- rs3093668G;Gcommon in complete genomicsTypical
- rs4645843C;Ccommon genotypeTypical
Notes
From SNPedia
Show notes, about 120 words
Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease. Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis. Family-based analysis of tumor necrosis factor and lymphotoxin-alpha tag polymorphisms with type 1 diabetes in the population of South Croatia. Association of MICA with rheumatoid arthritis independent of known HLA-DRB1 risk alleles in a family-based and a case control study. Toll-like receptor signaling pathway variants and prostate cancer mortality. Evaluation of genetic susceptibility to childhood allergy and asthma in an African American urban population.
Source and license
Adapted from rs3093664 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.