Standard

Sleep apnea

ETV5 · rs78785910

Where this position leads

Condition: Pediatric Obstructive Sleep Apnea

rs78785910 Condition: Pediatric Obstructive Sleep Apnea Pediatric Obstructive Sleep Apnea Condition rs78785910 rs78785910 ETV5

What the study found

Who was studied 45,335 African American or Afro-Caribbean cases, 70,630 African American or Afro-Caribbean controls, 22,934 Hispanic or Latin American cases, 34,075 Hispanic or Latin American controls, 2,460 East Asian ancestry cases, 4,090 East Asian ancestry controls, 152,031 European ancestry cases, 278,027 European ancestry controls.

The effect Each copy of the G allele shifted the measure 0.0457 higher (95% confidence interval 0.033-0.058); p = 2 × 10−13.

How common The G allele had a frequency of about 86% in the people studied.

Where it sits Chromosome 3, band 3q27.2 — in an intron of ETV5.

What each result means

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

Questions about rs78785910

What is rs78785910?

rs78785910 is a single position in the genome, in or near the ETV5 gene. Published research associates it with sleep apnea. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs78785910 linked to?

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

Does having rs78785910 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 rs78785910 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

Sleep apnea (rs78785910). MyGeneLog™. https://www.mygenelog.com/variants/rs78785910

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