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Sleep end time

LINC02260 · rs6833573

What the study found

Who was studied 90,515 individuals.

The effect Each copy of the C allele shifted the measure 0.515 lower (95% confidence interval 0.35-0.68); p = 2 × 10−9.

Where it sits Chromosome 4, band 4q12 — between genes, 23.7 kb from LINC02260.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Sleep end time compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Sleep end time.
T/T Published research associates this genotype with typical/baseline likelihood of Sleep end time — no copies of the reported risk allele.
Source

Questions about rs6833573

What is rs6833573?

rs6833573 is a single position in the genome, in or near the LINC02260 gene. Published research associates it with sleep end time. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6833573 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 rs6833573 come from?

GWAS Catalog, PLoS Genet 2020, PMID:33075057. 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 end time (rs6833573). MyGeneLog™. https://www.mygenelog.com/variants/rs6833573

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