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Breakfast cereal skipping frequency

METTL4 · rs8097544

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What the study found

Who was studied 193,860 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0326 higher (95% confidence interval 0.025-0.04); p = 2 × 10⁻¹⁷.

How common The G allele had a frequency of about 15% in the people studied.

Where it sits Chromosome 18, band 18p11.32 — between genes, 88.2 kb from AIDAP3.

What each result means

A/A No copy of the version the research linked to Breakfast cereal skipping frequency. This is the starting point the study compared everyone against.

A/G One copy of the version the research linked to Breakfast cereal skipping frequency. That is a smaller link than two copies.

G/G Two copies of the version the research linked to Breakfast cereal skipping frequency. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

Genome-wide association study of breakfast skipping links clock regulation with food timing

Dashti HS, Merino J, Lane JM, Song Y, Smith CE, Tanaka T, McKeown NM, Tucker C, Sun D, Bartz TM, Li-Gao R, Nisa H

and 15 more — show all

Reutrakul S, Lemaitre RN, Alshehri TM, de Mutsert R, Bazzano L, Qi L, Knutson KL, Psaty BM, Mook-Kanamori DO, Perica VB, Neuhouser ML, Scheer FAJL, Rutter MK, Garaulet M, Saxena R

The American journal of clinical nutrition · 2019 · PMID 31190057

Questions about rs8097544

What is rs8097544?

rs8097544 is a single position in the genome, in or near the METTL4 gene. Published research associates it with breakfast cereal skipping frequency. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs8097544 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 rs8097544 come from?

GWAS Catalog, The American journal of clinical nutrition 2019, PMID:31190057. 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.

Breakfast cereal skipping frequency (rs8097544). MyGeneLog™. https://www.mygenelog.com/variants/rs8097544

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