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Chronotype

PRR7 · rs465670

What the study found

Who was studied 449,734 European ancestry individuals; replicated in 248,098 European ancestry individuals.

The effect The reported allele is T; the catalogue records no effect size ; p = 3 × 10−10.

How common The T allele had a frequency of about 54% in the people studied.

Where it sits Chromosome 5, band 5q35.3 — in an intron of PRR7.

What each result means

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

Questions about rs465670

What is rs465670?

rs465670 is a single position in the genome, in or near the PRR7 gene. Published research associates it with chronotype. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs465670 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 rs465670 come from?

GWAS Catalog, Nature communications 2019, PMID:30696823. 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.

Chronotype (rs465670). MyGeneLog™. https://www.mygenelog.com/variants/rs465670

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