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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 2,935 Qatari ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.638 lower (95% confidence interval 0.55-0.73); p = 1 × 10−41.
How common The T allele had a frequency of about 9% in the people studied.
Where it sits Chromosome 12, band 12p13.31 — in an intron of C1S.
What each result means
A/ANo copy of the version the research linked to Complement C1q subcomponent levels. This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to Complement C1q subcomponent levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Complement C1q subcomponent levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs16933084
What is rs16933084?
rs16933084 is a single position in the genome, in or near the C1S gene. Published research associates it with complement c1q subcomponent levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs16933084 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 rs16933084 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. 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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