Sensitive

Parkinson's disease

COMMD1 · rs528521148

Where this position leads

Condition: Parkinson's Disease

rs528521148 Condition: Parkinson's Disease Parkinson's Disease Condition rs528521148 rs528521148 COMMD1

What the study found

Who was studied 278 African American or Afro-Caribbean cases, 55,227 African American or Afro-Caribbean controls, 4,047 European ancestry cases, 311,621 European ancestry controls, 235 Hispanic or Latin American cases, 29,079 Hispanic or Latin American controls.

The effect Each copy of the C allele shifted the measure 0.993 lower (95% confidence interval 0.9-1.09); p = 1 × 10−11.

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

Where it sits Chromosome 2, band 2p15 — in an intron of COMMD1.

What each result means

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

Questions about rs528521148

What is rs528521148?

rs528521148 is a single position in the genome, in or near the COMMD1 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 rs528521148 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 rs528521148 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 rs528521148 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

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 (rs528521148). MyGeneLog™. https://www.mygenelog.com/variants/rs528521148

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