Standard

Educational attainment

DPYD · rs80216782

Where this position leads

Condition: Educational Attainment

Drug: Fluoropyrimidines

rs80216782 Condition: Educational Attainment Educational Attainment Condition Drug: Fluoropyrimidines Fluoropyrimidines Drug rs80216782 rs80216782 DPYD

What the study found

Who was studied 3,037,499 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.00906 lower (95% confidence interval 0.0061-0.012); p = 3 × 10−9.

How common The T allele had a frequency of about 14% in the people studied.

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

What each result means

C/C No copy of the version the research linked to Educational attainment. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Educational attainment. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Educational attainment. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs80216782

What is rs80216782?

rs80216782 is a single position in the genome, in or near the DPYD gene. Published research associates it with educational attainment. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs80216782 linked to?

On MyGeneLog this position is linked to Educational Attainment. The research behind each link, and its sources, are set out on that condition page.

Does rs80216782 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 rs80216782 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 rs80216782 come from?

GWAS Catalog, Nature genetics 2022, PMID:35361970. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Educational attainment (rs80216782). MyGeneLog™. https://www.mygenelog.com/variants/rs80216782

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