Standard

Fibromyalgia

CNNM2 · rs75970938

Where this position leads

Condition: Fibromyalgia

rs75970938 Condition: Fibromyalgia Fibromyalgia Condition rs75970938 rs75970938 CNNM2

What the study found

Who was studied 62,808 European ancestry cases, 1,377,716 European ancestry controls, 15,763 African ancestry cases, 165,196 African ancestry controls, 6,568 Latin American cases, 99,521 Latin American controls.

The effect Each copy of the T allele shifted the measure 0.056 higher (95% confidence interval 0.036-0.076); p = 1 × 10−8.

Where it sits Chromosome 10, band 10q24.32 — in an intron of CNNM2.

What each result means

C/C No copy of the version the research linked to Fibromyalgia. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Fibromyalgia. That is a smaller link than two copies.
T/T 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.
Source

Questions about rs75970938

What is rs75970938?

rs75970938 is a single position in the genome, in or near the CNNM2 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 rs75970938 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 rs75970938 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 rs75970938 come from?

GWAS Catalog, Nature communications 2026, PMID:42521668. 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 (rs75970938). MyGeneLog™. https://www.mygenelog.com/variants/rs75970938

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