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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 119,279 African American or Afro-Caribbean individuals, 57,954 Hispanic or Latin American individuals, 6,419 East Asian ancestry individuals, 425,535 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0238 higher (95% confidence interval 0.017-0.03); p = 1 × 10−12.
How common The T allele had a frequency of about 61% in the people studied.
Where it sits Chromosome 5, band 5q34 — in an intron of TENM2.
What each result means
C/CNo copy of the version the research linked to Weight (mean, inv-normal transformed). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Weight (mean, inv-normal transformed). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Weight (mean, inv-normal 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 rs1345735
What is rs1345735?
rs1345735 is a single position in the genome, in or near the TENM2 gene. Published research associates it with weight (mean, inv-normal transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1345735 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 rs1345735 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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