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Hypothyroidism

CAPZB · rs12042240

Where this position leads

Condition: Hypothyroidism

rs12042240 Condition: Hypothyroidism Hypothyroidism Condition rs12042240 rs12042240 CAPZB

What the study found

Who was studied 12,258 admixed American cases, 106,876 admixed American controls.

The effect Each copy of the G allele shifted the measure 0.104 higher (95% confidence interval 0.074-0.134); p = 6 × 10−12.

How common The G allele had a frequency of about 33% in the people studied.

Where it sits Chromosome 1, band 1p36.13 — in an intron of CAPZB.

What each result means

A/A No copy of the version the research linked to Hypothyroidism. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Hypothyroidism. That is a smaller link than two copies.
G/G 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 rs12042240

What is rs12042240?

rs12042240 is a single position in the genome, in or near the CAPZB 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 rs12042240 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 rs12042240 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 rs12042240 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 (rs12042240). MyGeneLog™. https://www.mygenelog.com/variants/rs12042240

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