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Survival in progressive supranuclear palsy

SLC2A13 · rs2242367

What the study found

Who was studied 1,001 European ancestry individuals; replicated in 415 European ancestry individuals.

The effect Each copy of the A allele carried 1.37 times the odds of Survival in progressive supranuclear palsy (95% confidence interval 1.25-1.51); p = 1 × 10−10.

How common The A allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 12, band 12q12 — in an intron of SLC2A13.

What each result means

A/A Two copies of the version the research linked to Survival in progressive supranuclear palsy. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Survival in progressive supranuclear palsy. That is a smaller link than two copies.
G/G No copy of the version the research linked to Survival in progressive supranuclear palsy. This is the starting point the study compared everyone against.
Source

Questions about rs2242367

What is rs2242367?

rs2242367 is a single position in the genome, in or near the SLC2A13 gene. Published research associates it with survival in progressive supranuclear palsy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2242367 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 rs2242367 come from?

GWAS Catalog, The Lancet. Neurology 2021, PMID:33341150. 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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Survival in progressive supranuclear palsy (rs2242367). MyGeneLog™. https://www.mygenelog.com/variants/rs2242367

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