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Psoriatic arthropathy (PheCode 696.42)

GSTA5 · rs538519116

Where this position leads

Condition: Psoriatic Arthropathy

rs538519116 Condition: Psoriatic Arthropathy Psoriatic Arthropathy Condition rs538519116 rs538519116 GSTA5

What the study found

Who was studied 228 African American or Afro-Caribbean cases, 121,622 African American or Afro-Caribbean controls, 3,087 European ancestry cases, 447,533 European ancestry controls, 408 Hispanic or Latin American cases, 59,421 Hispanic or Latin American controls.

The effect Each copy of the C allele shifted the measure 4.33 lower (95% confidence interval 4.32-4.34); p = 5 × 10−13.

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

Where it sits Chromosome 6, band 6p12.2 — in an intron of GSTA5.

What each result means

C/C Two copies of the version the research linked to Psoriatic arthropathy (PheCode 696.42). 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 Psoriatic arthropathy (PheCode 696.42). That is a smaller link than two copies.
T/T No copy of the version the research linked to Psoriatic arthropathy (PheCode 696.42). This is the starting point the study compared everyone against.
Source

Questions about rs538519116

What is rs538519116?

rs538519116 is a single position in the genome, in or near the GSTA5 gene. Published research associates it with psoriatic arthropathy (phecode 696.42). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs538519116 linked to?

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

Does having rs538519116 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 rs538519116 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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Psoriatic arthropathy (PheCode 696.42) (rs538519116). MyGeneLog™. https://www.mygenelog.com/variants/rs538519116

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