Standard

Pediatric obstructive sleep apnea

HDDC3 · rs17593311

Where this position leads

Condition: Pediatric Obstructive Sleep Apnea

rs17593311 Condition: Pediatric Obstructive Sleep Apnea Pediatric Obstructive Sleep Apnea Condition rs17593311 rs17593311 HDDC3

What the study found

Who was studied 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 C; the catalogue records no effect size ; p = 5 × 10−8.

How common The C allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 15, band 15q26.1 — in an intron of MAN2A2.

What each result means

C/C 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.
C/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 rs17593311

What is rs17593311?

rs17593311 is a single position in the genome, in or near the HDDC3 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 rs17593311 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 rs17593311 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 rs17593311 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 (rs17593311). MyGeneLog™. https://www.mygenelog.com/variants/rs17593311

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