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Putamen iron levels (quantitative susceptibility mapping)

near HCG15 · rs184771565

What the study found

Who was studied 39,533 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.377 lower (95% confidence interval 0.26-0.5); p = 1 × 10−11.

Where it sits Chromosome 6, band 6p22.1 — between genes, 3.3 kb from HCG15.

What each result means

C/C No copy of the version the research linked to Putamen iron levels (quantitative susceptibility mapping). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Putamen iron levels (quantitative susceptibility mapping). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Putamen iron levels (quantitative susceptibility mapping). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs184771565

What is rs184771565?

rs184771565 is a single position in the genome, in or near the near HCG15 gene. Published research associates it with putamen 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 rs184771565 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 rs184771565 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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Putamen iron levels (quantitative susceptibility mapping) (rs184771565). MyGeneLog™. https://www.mygenelog.com/variants/rs184771565

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