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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 269,545 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0768 lower (95% confidence interval 0.058-0.095); p = 3 × 10−16.
Where it sits Chromosome 2, band 2p24.1 — in an intron of LDAH.
What each result means
C/CTwo copies of the version the research linked to LDL (standard GWA). 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 LDL (standard GWA). That is a smaller link than two copies.
T/TNo copy of the version the research linked to LDL (standard GWA). This is the starting point the study compared everyone against.
Nature human behaviour · 2023 · PMID 37106081 · open access
Questions about rs79800183
What is rs79800183?
rs79800183 is a single position in the genome, in or near the LDAH gene. Published research associates it with ldl (standard gwa). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs79800183 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 rs79800183 come from?
GWAS Catalog, Nature human behaviour 2023, PMID:37106081. 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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