rs6684439
A SNP in the IL6R gene on chromosome 1. Its most notable genotype is C;C: normal
- Gene
- IL6R
- Location
- Chr 1154,423,363 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 38%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageC;C 41% C;T 45% T;T 14%
- European ancestry (Utah)C;C 43% C;T 44% T;T 12%
- Han Chinese (Beijing)C;C 34% C;T 51% T;T 15%
- Japanese (Tokyo)C;C 43% C;T 43% T;T 15%
- Yoruba (Nigeria)C;C 37% C;T 50% T;T 14%
- African ancestry (Southwest US)C;C 40% C;T 44% T;T 16%
- Chinese (Denver)C;C 33% C;T 44% T;T 23%
- Gujarati IndianC;C 47% C;T 48% T;T 6%
- Luhya (Kenya)C;C 46% C;T 48% T;T 6%
- Mexican ancestry (Los Angeles)C;C 29% C;T 40% T;T 31%
- Maasai (Kenya)C;C 63% C;T 33% T;T 4%
- TuscanC;C 36% C;T 50% T;T 14%
Related
Conditions, medicines and genes
Other IL6R SNPs
- rs4845618G;T1.7x increased melanoma riskMinor
- rs7529229C;C2.5x higher risk of multiple myeloma than AAMinor
- rs4129267T;TAssociated with 73% higher IL-R and CRP levelsMinor
- rs2228145A;Acommon in clinvarTypical
- rs2229238C;Ccommon in complete genomicsTypical
- rs4845622A;AnormalTypical
- rs8192284A;Areduced risk of multiple myelomaTypical
Notes
From SNPedia
Notes
A study of 219 female melanoma patients and an equal number of controls concluded that 4 linked SNPs within the IL6R gene were associated with increased melanoma risk, but only when heterozygous. [Note that there may have been too few minor allele homozygotes to study, though.] The odds ratio associated with the minor allele of this SNP, rs6684439, was 1.74 (CI: 1.07-2.81). The 4 linked SNPs from identified in this study are: rs6684439, rs4845618, rs4845622, and rs8192284.
Source and license
Adapted from rs6684439 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.