Sensitive

Parkinson's disease

near SEC23IP · rs118117788

Where this position leads

Condition: Parkinson's Disease

rs118117788 Condition: Parkinson's Disease Parkinson's Disease Condition rs118117788 rs118117788 near SEC23IP

What the study found

Who was studied 57,893 European ancestry cases, 1,505,102 European ancestry controls, 7,046 East Asian ancestry cases, 176,756 East Asian ancestry controls, 2,440 Hispanic or Latin American cases, 582,220 Hispanic or Latin American controls, 288 African ancestry cases, 193,985 African ancestry controls.

The effect The reported allele is T; the catalogue records no effect size ; p = 4 × 10−23.

Where it sits Chromosome 10, band 10q26.12 — between genes, 6.3 kb from SEC23IP.

What each result means

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

Questions about rs118117788

What is rs118117788?

rs118117788 is a single position in the genome, in or near the near SEC23IP gene. Published research associates it with parkinson's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs118117788 linked to?

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

Does having rs118117788 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 rs118117788 come from?

GWAS Catalog, Nature genetics 2024, PMID:38155330. 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.

Parkinson's disease (rs118117788). MyGeneLog™. https://www.mygenelog.com/variants/rs118117788

← See all variants