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INHBB protein levels

near LINC01101 · rs146999772

Where this position leads

Condition: Celiac Disease

rs146999772 Condition: Celiac Disease Celiac Disease Condition rs146999772 rs146999772 near LINC011…

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.186 higher (95% confidence interval 0.13-0.24); p = 9 × 10−13.

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

Where it sits Chromosome 2, band 2q14.2 — between genes, 87.2 kb from LINC01101.

What each result means

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

Questions about rs146999772

What is rs146999772?

rs146999772 is a single position in the genome, in or near the near LINC01101 gene. Published research associates it with inhbb protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs146999772 linked to?

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

Does having rs146999772 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 rs146999772 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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.

INHBB protein levels (rs146999772). MyGeneLog™. https://www.mygenelog.com/variants/rs146999772

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