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Hypothyroidism

FKBP5 · rs4713911

Where this position leads

Conditions: Hypothyroidism, Thyroid Stimulating Hormone (TSH) Levels

rs4713911 Condition: Hypothyroidism Hypothyroidism Condition Condition: Thyroid Stimulating Hormone (TSH) Levels Thyroid Stimulating Hormone (TSH) Levels Condition rs4713911 rs4713911 FKBP5

What the study found

Who was studied 98,805 European ancestry cases, 948,186 European ancestry controls, 14,588 cases, 117,082 controls; replicated in 34,835 European ancestry cases, 492,149 European ancestry controls.

The effect Each copy of the C allele shifted the measure 0.05 higher (95% confidence interval 0.04-0.06); p = 1 × 10−21.

How common The C allele had a frequency of about 69% in the people studied.

Where it sits Chromosome 6, band 6p21.31 — inside FKBP5.

What each result means

C/C 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.
C/T One copy of the version the research linked to Hypothyroidism. That is a smaller link than two copies.
T/T No copy of the version the research linked to Hypothyroidism. This is the starting point the study compared everyone against.
Source

Questions about rs4713911

What is rs4713911?

rs4713911 is a single position in the genome, in or near the FKBP5 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 rs4713911 linked to?

On MyGeneLog this position is linked to Hypothyroidism, Thyroid Stimulating Hormone (TSH) Levels. The research behind each link, and its sources, are set out on that condition page.

Does having rs4713911 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 rs4713911 come from?

GWAS Catalog, Nature genetics 2025, PMID:41238958. 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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Hypothyroidism (rs4713911). MyGeneLog™. https://www.mygenelog.com/variants/rs4713911

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