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Pallidum iron levels (quantitative susceptibility mapping)

near UBQLN1P1 · rs2844745

What the study found

Who was studied 39,533 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0457 higher (95% confidence interval 0.032-0.059); p = 9 × 10−12.

Where it sits Chromosome 6, band 6p22.1 — between genes, 11.6 kb from UBQLN1P1.

What each result means

C/C Two copies of the version the research linked to Pallidum iron levels (quantitative susceptibility mapping). 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 Pallidum iron levels (quantitative susceptibility mapping). That is a smaller link than two copies.
T/T No copy of the version the research linked to Pallidum iron levels (quantitative susceptibility mapping). This is the starting point the study compared everyone against.
Source

Questions about rs2844745

What is rs2844745?

rs2844745 is a single position in the genome, in or near the near UBQLN1P1 gene. Published research associates it with pallidum iron levels (quantitative susceptibility mapping). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2844745 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 rs2844745 come from?

GWAS Catalog, Neurobiology of disease 2024, PMID:38789058. 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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Pallidum iron levels (quantitative susceptibility mapping) (rs2844745). MyGeneLog™. https://www.mygenelog.com/variants/rs2844745

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