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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 39,533 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.058 higher (95% confidence interval 0.038-0.078); p = 3 × 10−9.
Where it sits Chromosome 14, band 14q22.1 — in an intron of DDHD1-DT.
What each result means
C/CTwo copies of the version the research linked to Substantia nigra iron levels (R2* MRI). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Substantia nigra iron levels (R2* MRI). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Substantia nigra iron levels (R2* MRI). This is the starting point the study compared everyone against.
Neurobiology of disease · 2024 · PMID 38789058 · open access
Questions about rs8008063
What is rs8008063?
rs8008063 is a single position in the genome, in or near the DDHD1-DT gene. Published research associates it with substantia nigra iron levels (r2* mri). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs8008063 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 rs8008063 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.
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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.
Substantia nigra iron levels (R2* MRI) (rs8008063). MyGeneLog™. https://www.mygenelog.com/variants/rs8008063