Standard

sodium (maximum, inv-norm transformed)

DPYD · rs2811198

Where this position leads

Drug: Fluoropyrimidines

rs2811198 Drug: Fluoropyrimidines Fluoropyrimidines Drug rs2811198 rs2811198 DPYD

What the study found

Who was studied 118,412 African American or Afro-Caribbean individuals, 57,401 Hispanic or Latin American individuals, 6,311 East Asian ancestry individuals, 421,132 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0249 lower (95% confidence interval 0.018-0.032); p = 6 × 10−13.

How common The A allele had a frequency of about 88% in the people studied.

Where it sits Chromosome 1, band 1p21.3 — in an intron of DPYD.

What each result means

A/A Two copies of the version the research linked to sodium (maximum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to sodium (maximum, inv-norm transformed). That is a smaller link than two copies.
G/G No copy of the version the research linked to sodium (maximum, inv-norm transformed). This is the starting point the study compared everyone against.
Source

Questions about rs2811198

What is rs2811198?

rs2811198 is a single position in the genome, in or near the DPYD gene. Published research associates it with sodium (maximum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does rs2811198 affect how medicines work?

DPYD carries pharmacogenomic findings for Fluoropyrimidines. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.

Does having rs2811198 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs2811198 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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sodium (maximum, inv-norm transformed) (rs2811198). MyGeneLog™. https://www.mygenelog.com/variants/rs2811198

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