Sensitive

Parkinson’s disease progression to dementia

LRP1B · rs80306347

What the study found

Who was studied 3,923 European ancestry individuals.

The effect Each copy of the C allele carried 3.23 times the odds of Parkinson’s disease progression to dementia (95% confidence interval 2.17-4.81); p = 7 × 10−9.

Where it sits Chromosome 2, band 2q22.1 — in an intron of LRP1B.

What each result means

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

Questions about rs80306347

What is rs80306347?

rs80306347 is a single position in the genome, in or near the LRP1B gene. Published research associates it with parkinson’s disease progression to dementia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs80306347 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 rs80306347 come from?

GWAS Catalog, Brain : a journal of neurology 2023, PMID:36348503. 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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Parkinson’s disease progression to dementia (rs80306347). MyGeneLog™. https://www.mygenelog.com/variants/rs80306347

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