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Hypothyroidism

SPTBN4 · rs545497890

Where this position leads

Condition: Hypothyroidism

rs545497890 Condition: Hypothyroidism Hypothyroidism Condition rs545497890 rs545497890 SPTBN4

What the study found

Who was studied 257,365 African ancestry, admixed American, East Asian ancestry, European ancestry, South Asian ancestry, Greater Middle Eastern cases, 2,186,763 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 0.224 higher (95% confidence interval 0.16-0.29); p = 2 × 10−11.

How common The T allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 19, band 19q13.2 — in the 3′ untranslated region of SPTBN4.

What each result means

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

Questions about rs545497890

What is rs545497890?

rs545497890 is a single position in the genome, in or near the SPTBN4 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 rs545497890 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 rs545497890 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 rs545497890 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.

Hypothyroidism (rs545497890). MyGeneLog™. https://www.mygenelog.com/variants/rs545497890

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