rs17824933

A SNP in the CD6 gene on chromosome 11. Its most notable genotype is C;C: common on affy axiom data

Gene
CD6
Location
Chr 1160,993,140 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
11%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon on affy axiom dataTypical · 0.090% of people

On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageC;C 90%
  • European ancestry (Utah)C;C 63%
  • Han Chinese (Beijing)C;C 98%
  • Japanese (Tokyo)C;C 98%
  • Yoruba (Nigeria)C;C 100%

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs17824933 is a SNP in the region of the CD6 gene. A large study (~5,000 patients) found an increased risk for multiple sclerosis associated with rs17824933; the odds ratio for the minor allele was reported as 1.18 (CI: 1.07-1.30, p=3.79x10(-9)).

Source and license

Adapted from rs17824933 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.