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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 6,246 Han Chinese ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.108 lower (95% confidence interval 0.073-0.143); p = 2 × 10−9.
How common The C allele had a frequency of about 32% in the people studied.
Where it sits Chromosome 6, band 6q15 — in an intron of RNGTT.
What each result means
C/CTwo copies of the version the research linked to Apnea hypopnea index. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Apnea hypopnea index. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Apnea hypopnea index. This is the starting point the study compared everyone against.
American journal of respiratory and critical care medicine · 2022 · PMID 35819321
Questions about rs2610711
What is rs2610711?
rs2610711 is a single position in the genome, in or near the RNGTT gene. Published research associates it with apnea hypopnea index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2610711 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 rs2610711 come from?
GWAS Catalog, American journal of respiratory and critical care medicine 2022, PMID:35819321. 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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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.
Apnea hypopnea index (rs2610711). MyGeneLog™. https://www.mygenelog.com/variants/rs2610711