Sensitive

Graves' disease

RAD51B · rs74435447

Where this position leads

Condition: Graves' Disease

rs74435447 Condition: Graves' Disease Graves' Disease Condition rs74435447 rs74435447 RAD51B

What the study found

Who was studied 18,719 African ancestry, admixed American, East Asian ancestry, European ancestry, South Asian ancestry, Greater Middle Eastern cases, 2,441,938 African ancestry, admixed American, East Asian ancestry, European ancestry, South Asian ancestry, Greater Middle Eastern controls.

The effect Each copy of the T allele shifted the measure 0.312 lower (95% confidence interval 0.2-0.42); p = 3 × 10−8.

How common The T allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 14, band 14q24.1 — in an intron of RAD51B.

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 rs74435447

What is rs74435447?

rs74435447 is a single position in the genome, in or near the RAD51B 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 rs74435447 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 rs74435447 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 rs74435447 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 (rs74435447). MyGeneLog™. https://www.mygenelog.com/variants/rs74435447

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