Sensitive

Graves' disease

LINC02980 · rs775179965

Where this position leads

Condition: Graves' Disease

rs775179965 Condition: Graves' Disease Graves' Disease Condition rs775179965 rs775179965 LINC02980

What the study found

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

The effect Each copy of the T allele shifted the measure 1.01 higher (95% confidence interval 0.65-1.37); p = 4 × 10−8.

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

Where it sits Chromosome 6, band 6p22.2 — in an intron of LINC02980.

What each result means

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

Questions about rs775179965

What is rs775179965?

rs775179965 is a single position in the genome, in or near the LINC02980 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 rs775179965 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 rs775179965 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 rs775179965 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 (rs775179965). MyGeneLog™. https://www.mygenelog.com/variants/rs775179965

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