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Ease of getting up in the morning

TNFSF4 · rs148137538

What the study found

Who was studied 385,949 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0389 higher (95% confidence interval 0.03-0.048); p = 1 × 10−11.

How common The G allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 1, band 1q25.1 — in an intron of TNFSF4.

What each result means

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

Questions about rs148137538

What is rs148137538?

rs148137538 is a single position in the genome, in or near the TNFSF4 gene. Published research associates it with ease of getting up in the morning. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs148137538 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 rs148137538 come from?

GWAS Catalog, Nature genetics 2019, PMID:30804565. 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.

Ease of getting up in the morning (rs148137538). MyGeneLog™. https://www.mygenelog.com/variants/rs148137538

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