rs34815109

A SNP in the UGT1A10 gene on chromosome 2. Its most notable genotype is -;-: normal

Gene
UGT1A10
Location
Chr 2233,760,234 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. -;-Most notableNot ratednormalTypical · 0.0
  2. -;TANot ratedsome effects of higher bilirubinTypical · 0.0
  3. TA;TANot ratedeffects of higher bilirubin; irinotecan toxicity; tranilast toxicityTypical · 0.0

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

Notes

From SNPedia

Show notes, about 380 words

Although the insertion is supposed to be the minor allele, the majority of FTDNA v2 and 23andMe v2 results show II as the result, so use caution when interpreting this result. rs34815109 is one of four SNPs all describing an insertion/deletion polymorphism in the promoter region of the UGT1A1 gene. This gene encodes a protein that modifies hepatic bilirubin in order to allow it to be excreted. SNPs that reduce the activity of the UGT1A1 gene therefore tend to increase serum bilirubin levels. The rs34815109(TA) allele represents the insertion variant, which actually adds a seventh (TA) pair to what is already a string of six (TA) pairs; this reduces the activity to 30% of normal, and is thus the risk allele. The risk allele is commonly referred to as the UGT1A1*28 allele, and it is homozygous in ~10% of the US population. Risks associated with the rs34815109(TA) allele are almost always associated with the homozygous (TA;TA) genotype, with smaller (or no) effects seen for rs34815109(-;TA) heterozygous carriers. These risks include: * An increased risk for breast cancer is reported in premenopausal African-American women, based on a study of 200 women. The reported odds ratio was 1.8 (CI: 1.0-3.1, p=0.06) for carriers of one or more UGT1A1*28 alleles. * In colorectal cancer patients being treated with irinotecan, adverse side effects (neutropenia and/or severe diarrhea) are reported to be strongly associated with the number of UGT1A1*28 alleles. Patients homozygous for the *28 allele are 3.5 times more likely to develop severe neutropenia compared with individuals with the wild genotype. The FDA has approved a genetic test for UGT1A1 status to be used to determine dosage when considering irinotecan therapy http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2005/ucm108475.htm FDA press release. However, no prospective study has examined whether a reduced dose of irinotecan results in a reduced rate of adverse drug events. * Hyperbilirubinemia, a potentially toxic increase in bilirubin levels, is possible among rs34815109(TA;TA) individuals treated with the drug tranilast. The three other SNPs that describe the same polymorphism are: * rs34983651 * rs35600288 * rs5839491

TA;TA

http://web.me.com/russbaltman/Site/PharmGKBlog/Entries/2010/10/24_Updated_Irinotecan_Label.html

Source and license

Adapted from rs34815109 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.