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Walking pace

ADGRB2 · rs12739999

What the study found

Who was studied 450,967 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0116 higher (95% confidence interval 0.0084-0.0149); p = 3 × 10−12.

Where it sits Chromosome 1, band 1p35.2 — in an intron of ADGRB2.

What each result means

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

Questions about rs12739999

What is rs12739999?

rs12739999 is a single position in the genome, in or near the ADGRB2 gene. Published research associates it with walking pace. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12739999 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 rs12739999 come from?

GWAS Catalog, Communications biology 2020, PMID:33128006. 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.

Walking pace (rs12739999). MyGeneLog™. https://www.mygenelog.com/variants/rs12739999

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