Sensitive

Chronic fatigue syndrome (PheCode 798.1)

near RALYL · rs141691232

Where this position leads

Condition: Chronic Fatigue Syndrome (ME/CFS)

rs141691232 Condition: Chronic Fatigue Syndrome (ME/CFS) Chronic Fatigue Syndrome (ME/CFS) Condition rs141691232 rs141691232 near RALYL

What the study found

Who was studied 648 African American or Afro-Caribbean cases, 119,584 African American or Afro-Caribbean controls, 3,891 European ancestry cases, 439,202 European ancestry controls, 409 Hispanic or Latin American cases, 58,515 Hispanic or Latin American controls.

The effect Each copy of the G allele shifted the measure 2.5 lower (95% confidence interval 2.46-2.54); p = 6 × 10−13.

How common The G allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 8, band 8q21.2 — between genes, 101.1 kb from TPM3P3.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Chronic fatigue syndrome (PheCode 798.1) — no copies of the reported risk allele.
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Chronic fatigue syndrome (PheCode 798.1).
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Chronic fatigue syndrome (PheCode 798.1) compared to the general population.
Source

Questions about rs141691232

What is rs141691232?

rs141691232 is a single position in the genome, in or near the near RALYL gene. Published research associates it with chronic fatigue syndrome (phecode 798.1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs141691232 linked to?

On MyGeneLog this position is linked to Chronic Fatigue Syndrome (ME/CFS). The research behind each link, and its sources, are set out on that condition page.

Does having rs141691232 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 rs141691232 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Chronic fatigue syndrome (PheCode 798.1) (rs141691232). MyGeneLog™. https://www.mygenelog.com/variants/rs141691232

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