Sensitive

Hodgkin's disease (PheCode 201)

TTL · rs565643303

Where this position leads

Condition: Hodgkin's Disease

rs565643303 Condition: Hodgkin's Disease Hodgkin's Disease Condition rs565643303 rs565643303 TTL

What the study found

Who was studied 215 African American or Afro-Caribbean cases, 121,633 African American or Afro-Caribbean controls, 975 European ancestry cases, 449,793 European ancestry controls.

The effect Each copy of the G allele shifted the measure 3.25 lower (95% confidence interval 3.23-3.28); p = 2 × 10−12.

How common The G allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 2, band 2q14.1 — in the 3′ untranslated region of TTL.

What each result means

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hodgkin's disease (PheCode 201) compared to the general population.
G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hodgkin's disease (PheCode 201).
T/T Published research associates this genotype with typical/baseline likelihood of Hodgkin's disease (PheCode 201) — no copies of the reported risk allele.
Source

Questions about rs565643303

What is rs565643303?

rs565643303 is a single position in the genome, in or near the TTL gene. Published research associates it with hodgkin's disease (phecode 201). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs565643303 linked to?

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

Does having rs565643303 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 rs565643303 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.

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Hodgkin's disease (PheCode 201) (rs565643303). MyGeneLog™. https://www.mygenelog.com/variants/rs565643303

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