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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 3,713 Sub-Saharan African ancestry individuals, 1,846 African American individuals.
The effect
Each copy of the C allele shifted the measure 0.18 lower (95% confidence interval 0.12-0.24); p = 1 × 10−8.
Where it sits Chromosome 7, band 7q35 — in an intron of CNTNAP2.
What each result means
C/CTwo copies of the version the research linked to Adipsin levels. 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 Adipsin levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Adipsin levels. This is the starting point the study compared everyone against.
Genome medicine · 2021 · PMID 34620218 · open access
Questions about rs113529034
What is rs113529034?
rs113529034 is a single position in the genome, in or near the CNTNAP2 gene. Published research associates it with adipsin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs113529034 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 rs113529034 come from?
GWAS Catalog, Genome medicine 2021, PMID:34620218. 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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