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Age at onset of walking

near LINC02128 · rs4785475

What the study found

Who was studied 70,560 European ancestry children.

The effect Each copy of the A allele shifted the measure 0.081 higher (95% confidence interval 0.056-0.106); p = 1 × 10−9.

How common The A allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 16, band 16q12.1 — between genes, 4.8 kb from LINC02128.

What each result means

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

Questions about rs4785475

What is rs4785475?

rs4785475 is a single position in the genome, in or near the near LINC02128 gene. Published research associates it with age at onset of walking. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4785475 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 rs4785475 come from?

GWAS Catalog, Nature human behaviour 2025, PMID:40335706. 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.

Age at onset of walking (rs4785475). MyGeneLog™. https://www.mygenelog.com/variants/rs4785475

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