rs1800584

A SNP in the TPMT gene on chromosome 6. Its most notable genotype is T;T: TPMT*4A homozygote; likely issues detoxifying certain drugs

Gene
TPMT
Location
Chr 618,130,781 (GRCh38)
Highest magnitude
3.5Important
Tested on
23andMe, AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableBadTPMT*4A homozygote; likely issues detoxifying certain drugsImportant · 3.52% of people
  2. C;TBadTPMT*4A heterozygote; possible issues detoxifying certain drugsImportant · 3.098% of people
  3. C;CGoodcommon in complete genomicsTypical · 0.00% of people

SNPedia records rs1800584 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in one HapMap population.

  • European ancestry (Utah)T;T 2% C;T 98% C;C 0%

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs1800584 is a rare SNP in the TPMT gene, potentially encoding a variant incapable of detoxifying byproducts of certain antineoplastic and immunosuppressant drugs. In general, individuals must have two nonfunctioning TPMT alleles for the toxicity to be pronounced. The rs1800584(A) SNP defines the TPMT*4A allele (OMIM). wikipedia thiopurine drugs metabolized by TPMT include azathioprine, mercaptopurine, and thioguanine

Source and license

Adapted from rs1800584 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.