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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 73,039 African American or Afro-Caribbean individuals, 37,339 Hispanic or Latin American individuals, 3,873 East Asian ancestry individuals, 259,269 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0327 higher (95% confidence interval 0.024-0.042); p = 3 × 10−13.
How common The C allele had a frequency of about 85% in the people studied.
Where it sits Chromosome 13, band 13q34 — in an intron of COL4A1.
What each result means
A/ANo copy of the version the research linked to monocyte (absolute count, maximum, inv-norm transformed). This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to monocyte (absolute count, maximum, inv-norm transformed). That is a smaller link than two copies.
C/CTwo copies of the version the research linked to monocyte (absolute count, maximum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs16975420
What is rs16975420?
rs16975420 is a single position in the genome, in or near the COL4A1 gene. Published research associates it with monocyte (absolute count, maximum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs16975420 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 rs16975420 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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