Sensitive

Autoimmune thyroid disease

CLEC2D · rs76226393

Where this position leads

Condition: Autoimmune Thyroid Disease

rs76226393 Condition: Autoimmune Thyroid Disease Autoimmune Thyroid Disease Condition rs76226393 rs76226393 CLEC2D

What the study found

Who was studied 30,234 European ancestry cases, 724,172 European ancestry controls.

The effect Each copy of the T allele carried 1.09 times the odds of Autoimmune thyroid disease; p = 9 × 10−15.

How common The T allele had a frequency of about 74% in the people studied.

Where it sits Chromosome 12, band 12p13.31 — in an intron of CLEC2D.

What each result means

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

Questions about rs76226393

What is rs76226393?

rs76226393 is a single position in the genome, in or near the CLEC2D gene. Published research associates it with autoimmune thyroid 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 rs76226393 linked to?

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

Does having rs76226393 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 rs76226393 come from?

GWAS Catalog, Nature 2020, PMID:32581359. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Autoimmune thyroid disease (rs76226393). MyGeneLog™. https://www.mygenelog.com/variants/rs76226393

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