Standard

Pediatric obstructive sleep apnea

near SMCHD1 · rs114124196

Where this position leads

Condition: Pediatric Obstructive Sleep Apnea

rs114124196 Condition: Pediatric Obstructive Sleep Apnea Pediatric Obstructive Sleep Apnea Condition rs114124196 rs114124196 near SMCHD1

What the study found

Who was studied 688 European ancestry cases, 3,165 European ancestry controls, 798 African American or Afro-Caribbean, African ancestry cases, 3,796 African American or Afro-Caribbean, African ancestry controls.

The effect The reported allele is A; the catalogue records no effect size ; p = 2 × 10−8.

Where it sits Chromosome 18, band 18p11.32 — between genes, 1.1 kb from CBX3P2.

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 rs114124196

What is rs114124196?

rs114124196 is a single position in the genome, in or near the near SMCHD1 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 rs114124196 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 rs114124196 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 rs114124196 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

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.

Pediatric obstructive sleep apnea (rs114124196). MyGeneLog™. https://www.mygenelog.com/variants/rs114124196

← See all variants