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Height

TRIP11 · rs8007661

Where this position leads

Condition: Height

rs8007661 Condition: Height Height Condition rs8007661 rs8007661 TRIP11

What the study found

Who was studied 67,452 Han Chinese ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.045 higher (95% confidence interval 0.035-0.055); p = 1 × 10−18.

Where it sits Chromosome 14, band 14q32.12 — in an intron of TRIP11.

What ClinVar records

Classification Benign; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2018-06-14. ClinVar record 667809 NM_004239.4(TRIP11):c.5160+195G>A

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C Two copies of the version the research linked to Height. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Height. That is a smaller link than two copies.
T/T No copy of the version the research linked to Height. This is the starting point the study compared everyone against.
Source

Questions about rs8007661

What is rs8007661?

rs8007661 is a single position in the genome, in or near the TRIP11 gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs8007661 linked to?

On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.

Does having rs8007661 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 rs8007661 come from?

GWAS Catalog, BMC medicine 2022, PMID:35831902. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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 (rs8007661). MyGeneLog™. https://www.mygenelog.com/variants/rs8007661

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