Sensitive

Plantar fascial disorders

WWP2 · rs62051384

Where this position leads

Condition: Plantar Fascial Disorders

rs62051384 Condition: Plantar Fascial Disorders Plantar Fascial Disorders Condition rs62051384 rs62051384 WWP2

What the study found

Who was studied 17,627 European ancestry cases, 2,044 Latin American cases, 1,300 East Asian cases, 658 African American cases, 65,637 European ancestry controls, 6,516 Latin American controls, 6,218 East Asian controls, 2,508 African American controls.

The effect Each copy of the T allele carried 1.07 times the odds of Plantar fascial disorders (95% confidence interval 1.04-1.09); p = 2 × 10−8.

How common The T allele had a frequency of about 37% in the people studied.

Where it sits Chromosome 16, band 16q22.1 — in an intron of WWP2.

What each result means

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

Questions about rs62051384

What is rs62051384?

rs62051384 is a single position in the genome, in or near the WWP2 gene. Published research associates it with plantar fascial disorders. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs62051384 linked to?

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

Does having rs62051384 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 rs62051384 come from?

GWAS Catalog, Int J Sports Med 2018, PMID:29534260. 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.

Plantar fascial disorders (rs62051384). MyGeneLog™. https://www.mygenelog.com/variants/rs62051384

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