CTCF · rs117017165
Where this position leads
Condition: Height
What the study found
Who was studied 405,540 European ancestry individuals.
The effect Each copy of the G allele shifted the measure 0.0286 higher (95% confidence interval 0.023-0.035); p = 3 × 10−20.
How common The G allele had a frequency of about 96% in the people studied.
Where it sits Chromosome 16, band 16q22.1 — in an intron of CTCF.
rs117017165 is a single position in the genome, in or near the CTCF gene. Published research associates it with height (baseline). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Nature communications 2025, PMID:40374629. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Height (baseline) (rs117017165). MyGeneLog™. https://www.mygenelog.com/variants/rs117017165