Sensitive

Parkinson's disease-related grey matter volume atrophy

MOBP · rs1708104

Where this position leads

Condition: Parkinson's Disease

rs1708104 Condition: Parkinson's Disease Parkinson's Disease Condition rs1708104 rs1708104 MOBP

What the study found

Who was studied 35,098 European ancestry individuals.

The effect The reported allele is T; the catalogue records no effect size ; p = 3 × 10−9.

Where it sits Chromosome 3, band 3p22.1 — in an intron of MOBP.

What each result means

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

Questions about rs1708104

What is rs1708104?

rs1708104 is a single position in the genome, in or near the MOBP gene. Published research associates it with parkinson's disease-related grey matter volume atrophy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1708104 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 rs1708104 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 rs1708104 come from?

GWAS Catalog, NeuroImage 2026, PMID:42336304. 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-related grey matter volume atrophy (rs1708104). MyGeneLog™. https://www.mygenelog.com/variants/rs1708104

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