Standard

Accelerometer-based physical activity measurement (average acceleration)

MEF2C · rs17551090

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−9, with 1 associations in the GWAS Catalog.

How this is scored

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 91,084 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.34 milli-gravities higher; p = 3 × 10−9.

How common The T allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 5, band 5q14.3 — in an intron of MEF2C.

What each result means

A/A No copy of the version the research linked to Accelerometer-based physical activity measurement (average acceleration). This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to Accelerometer-based physical activity measurement (average acceleration). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Accelerometer-based physical activity measurement (average acceleration). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs17551090

What is rs17551090?

rs17551090 is a single position in the genome, in or near the MEF2C gene. Published research associates it with accelerometer-based physical activity measurement (average acceleration). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17551090 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 rs17551090 come from?

GWAS Catalog, International journal of obesity (2005) 2018, PMID:29899525. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Accelerometer-based physical activity measurement (average acceleration) (rs17551090). MyGeneLog™. https://www.mygenelog.com/variants/rs17551090

← See all variants