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Hypothyroidism

LPP · rs4686955

Where this position leads

Condition: Hypothyroidism

rs4686955 Condition: Hypothyroidism Hypothyroidism Condition rs4686955 rs4686955 LPP

What the study found

Who was studied 58,783 European ancestry cases, 633,203 European ancestry controls.

The effect Each copy of the A allele carried 1.12 times the odds of Hypothyroidism (95% confidence interval 1.1-1.13); p = 1 × 10−41.

Where it sits Chromosome 3, band 3q28 — in an intron of LPP.

What each result means

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

Questions about rs4686955

What is rs4686955?

rs4686955 is a single position in the genome, in or near the LPP gene. Published research associates it with hypothyroidism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs4686955 linked to?

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

Does having rs4686955 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 rs4686955 come from?

GWAS Catalog, European journal of endocrinology 2024, PMID:39067062. 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.

Hypothyroidism (rs4686955). MyGeneLog™. https://www.mygenelog.com/variants/rs4686955

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