Sensitive

Graves' disease

DHX16 · rs140943109

Where this position leads

Condition: Graves' Disease

rs140943109 Condition: Graves' Disease Graves' Disease Condition rs140943109 rs140943109 DHX16

What the study found

Who was studied 12,019 European ancestry cases, 1,869,646 European ancestry controls.

The effect Each copy of the C allele shifted the measure 1.37 higher (95% confidence interval 0.98-1.77); p = 1 × 10−11.

How common The C allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — in an intron of DHX16.

What each result means

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

Questions about rs140943109

What is rs140943109?

rs140943109 is a single position in the genome, in or near the DHX16 gene. Published research associates it with graves' disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs140943109 linked to?

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

Does having rs140943109 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 rs140943109 come from?

GWAS Catalog, Nature genetics 2026, PMID:41644669. 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.

Graves' disease (rs140943109). MyGeneLog™. https://www.mygenelog.com/variants/rs140943109

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