Standard

Height (baseline)

near E2F7 · rs190351178

Where this position leads

Condition: Height

rs190351178 Condition: Height Height Condition rs190351178 rs190351178 near E2F7

What the study found

Who was studied 405,540 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0261 higher (95% confidence interval 0.018-0.034); p = 6 × 10−11.

How common The G allele had a frequency of about 97% in the people studied.

Where it sits Chromosome 12, band 12q21.2 — between genes, 11 kb from E2F7.

What each result means

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

Questions about rs190351178

What is rs190351178?

rs190351178 is a single position in the genome, in or near the near E2F7 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.

What conditions is rs190351178 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 rs190351178 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 rs190351178 come from?

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.

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 (baseline) (rs190351178). MyGeneLog™. https://www.mygenelog.com/variants/rs190351178

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