CCDC91 · rs11700039
Where this position leads
Condition: Height
Strength of the evidence
Its strongest genetic-study result is p = 10−20, with 1 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 405,540 European ancestry individuals.
The effect Each copy of the C allele shifted the measure 0.0303 higher (95% confidence interval 0.024-0.037); p = 9 × 10−21.
How common The C allele had a frequency of about 94% in the people studied.
Where it sits Chromosome 12, band 12p11.22 — in an intron of CCDC91.
rs11700039 is a single position in the genome, in or near the CCDC91 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.
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Height (baseline) (rs11700039). MyGeneLog™. https://www.mygenelog.com/variants/rs11700039