Sensitive

Thyroid cancer

TTC28 · rs143459581

Where this position leads

Condition: Thyroid Cancer

rs143459581 Condition: Thyroid Cancer Thyroid Cancer Condition rs143459581 rs143459581 TTC28

What the study found

Who was studied 6,056 European ancestry cases, 907,977 European ancestry controls, 4,661 East Asian ancestry cases, 354,129 East Asian ancestry controls, 5,450 African, Admixed American, European, East Asian, South Asian or unknown ancestry cases, 1,168,268 African, Admixed American, European, East Asian, South Asian or unknown ancestry controls.

The effect Each copy of the T allele shifted the measure 0.586 higher (95% confidence interval 0.48-0.7); p = 2 × 10−25.

Where it sits Chromosome 22, band 22q12.1 — in an intron of TTC28.

What each result means

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

Questions about rs143459581

What is rs143459581?

rs143459581 is a single position in the genome, in or near the TTC28 gene. Published research associates it with thyroid cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs143459581 linked to?

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

Does having rs143459581 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 rs143459581 come from?

GWAS Catalog, Nature communications 2026, PMID:42431967. 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.

Thyroid cancer (rs143459581). MyGeneLog™. https://www.mygenelog.com/variants/rs143459581

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