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Glutamine levels

SFXN1 · rs34907038

What the study found

Who was studied 4,435 East Asian ancestry individuals, 11,340 South Asian ancestry individuals, 115,911 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.255 higher (95% confidence interval 0.19-0.32); p = 4 × 10−15.

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

Where it sits Chromosome 5, band 5q35.2 — a missense change in SFXN1.

What each result means

C/C No copy of the version the research linked to Glutamine levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Glutamine levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Glutamine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs34907038

What is rs34907038?

rs34907038 is a single position in the genome, in or near the SFXN1 gene. Published research associates it with glutamine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs34907038 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 rs34907038 come from?

GWAS Catalog, Nature 2024, PMID:38448586. 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.

Glutamine levels (rs34907038). MyGeneLog™. https://www.mygenelog.com/variants/rs34907038

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