Standard

Pediatric obstructive sleep apnea

ASAP2 · rs72775219

Where this position leads

Condition: Pediatric Obstructive Sleep Apnea

rs72775219 Condition: Pediatric Obstructive Sleep Apnea Pediatric Obstructive Sleep Apnea Condition rs72775219 rs72775219 ASAP2

What the study found

Who was studied 433 European ancestry male cases, 1,586 European ancestry male controls, 427 African American or Afro-Caribbean, African ancestry male cases, 1,895 African American or Afro-Caribbean, African ancestry male controls.

The effect The reported allele is A; the catalogue records no effect size ; p = 8 × 10−9.

Where it sits Chromosome 2, band 2p25.1 — in an intron of ASAP2.

What each result means

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

Questions about rs72775219

What is rs72775219?

rs72775219 is a single position in the genome, in or near the ASAP2 gene. Published research associates it with pediatric obstructive 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 rs72775219 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 rs72775219 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 rs72775219 come from?

GWAS Catalog, Sleep 2024, PMID:35902206. 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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Pediatric obstructive sleep apnea (rs72775219). MyGeneLog™. https://www.mygenelog.com/variants/rs72775219

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