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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 6,136 Finnish ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.6 lower; p = 6 × 10−16.
Where it sits Chromosome 16, band 16p12.3 — in an intron of DNAH3.
What each result means
C/CTwo copies of the version the research linked to X-17676 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to X-17676 levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to X-17676 levels. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35347128 · open access
Questions about rs185603444
What is rs185603444?
rs185603444 is a single position in the genome, in or near the DNAH3 gene. Published research associates it with x-17676 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs185603444 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 rs185603444 come from?
GWAS Catalog, Nature communications 2022, PMID:35347128. 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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