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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 2,935 Qatari ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.283 lower (95% confidence interval 0.22-0.35); p = 5 × 10−17.
How common The C allele had a frequency of about 19% in the people studied.
Where it sits Chromosome 3, band 3p21.31 — a synonymous change in LTF.
What each result means
C/CTwo copies of the version the research linked to Teratocarcinoma-derived growth factor 1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Teratocarcinoma-derived growth factor 1 levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Teratocarcinoma-derived growth factor 1 levels. This is the starting point the study compared everyone against.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs2239692
What is rs2239692?
rs2239692 is a single position in the genome, in or near the LTF gene. Published research associates it with teratocarcinoma-derived growth factor 1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2239692 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 rs2239692 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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