Standard

Fibromyalgia

near LINC02607 · rs34683740

Where this position leads

Condition: Fibromyalgia

rs34683740 Condition: Fibromyalgia Fibromyalgia Condition rs34683740 rs34683740 near LINC026…

What the study found

Who was studied 2,313,287 European ancestry individuals, 119,673 African ancestry individuals, 52,716 South Asian ancestry individuals, 78,079 Hispanic or Latin American individuals.

The effect Each copy of the C allele carried 1.07 times the odds of Fibromyalgia (95% confidence interval 1.046-1.1); p = 4 × 10−8.

How common The C allele had a frequency of about 7% in the people studied.

Where it sits Chromosome 1, band 1p21.3 — between genes, 60.7 kb from LINC02607.

What each result means

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

Questions about rs34683740

What is rs34683740?

rs34683740 is a single position in the genome, in or near the near LINC02607 gene. Published research associates it with fibromyalgia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs34683740 linked to?

On MyGeneLog this position is linked to Fibromyalgia. The research behind each link, and its sources, are set out on that condition page.

Does having rs34683740 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 rs34683740 come from?

GWAS Catalog, Nature medicine 2026, PMID:42521817. 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.

Fibromyalgia (rs34683740). MyGeneLog™. https://www.mygenelog.com/variants/rs34683740

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