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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 18,532 European ancestry individuals, 1,142 African American individuals.
The effect
The reported allele is C; the catalogue records no effect size
; p = 1 × 10−10.
Where it sits Chromosome 1, band 1p32.1 — in an intron of FGGY.
What each result means
C/CTwo copies of the version the research linked to Neurofilament light chain levels. 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 Neurofilament light chain levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Neurofilament light chain levels. This is the starting point the study compared everyone against.
Communications biology · 2024 · PMID 39251807 · open access
Questions about rs11583796
What is rs11583796?
rs11583796 is a single position in the genome, in or near the FGGY gene. Published research associates it with neurofilament light chain levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11583796 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 rs11583796 come from?
GWAS Catalog, Communications biology 2024, PMID:39251807. 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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