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Transforming growth factor-beta-induced protein ig-h3 levels

near VTRNA2-1 · rs7728385

What the study found

Who was studied 3,506 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.235 lower (95% confidence interval 0.17-0.3); p = 4 × 10−11.

How common The T allele had a frequency of about 11% in the people studied.

Where it sits Chromosome 5, band 5q31.1 — between genes, 2.8 kb from VTRNA2-1.

What each result means

G/G No copy of the version the research linked to Transforming growth factor-beta-induced protein ig-h3 levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Transforming growth factor-beta-induced protein ig-h3 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Transforming growth factor-beta-induced protein ig-h3 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs7728385

What is rs7728385?

rs7728385 is a single position in the genome, in or near the near VTRNA2-1 gene. Published research associates it with transforming growth factor-beta-induced protein ig-h3 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7728385 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 rs7728385 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. 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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Transforming growth factor-beta-induced protein ig-h3 levels (rs7728385). MyGeneLog™. https://www.mygenelog.com/variants/rs7728385

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