rs2117032

A SNP on chromosome 12. Its most notable genotype is C;C: increase of 0.096 mg/dl in bilirubin levels

Gene
None listed
Location
Chr 1220,921,188 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
48%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableBadincrease of 0.096 mg/dl in bilirubin levelsTypical · 0.038% of people
  2. C;TBadincrease of 0.048 mg/dl in bilirubin levelsTypical · 0.038% of people

On SNPedia: (C;C), (C;T). 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 38% C;T 38%
  • European ancestry (Utah)C;C 11% C;T 54%
  • Han Chinese (Beijing)C;C 20% C;T 58%
  • Japanese (Tokyo)C;C 23% C;T 39%
  • Yoruba (Nigeria)C;C 97% C;T 3%

Source and license

Adapted from rs2117032 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.