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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 3,444 European ancestry individuals; replicated in 3,230 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.015 nmol/l lower (95% confidence interval 0.011-0.019); p = 1 × 10−12.
How common The G allele had a frequency of about 40% in the people studied.
Where it sits Chromosome 11, band 11p15.4 — in an intron of AMPD3.
What each result means
A/ANo copy of the version the research linked to Circulating vasoactive peptide levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Circulating vasoactive peptide levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Circulating vasoactive peptide levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs2957692 is a single position in the genome, in or near the ADM gene. Published research associates it with circulating vasoactive peptide levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2957692 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 rs2957692 come from?
GWAS Catalog, Hypertension (Dallas, Tex. : 1979) 2013, PMID:23381795. 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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Quoting this page
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