Standard

Hip circumference adjusted for BMI

DLEU1 · rs201770

Where this position leads

Condition: Hip Circumference

rs201770 Condition: Hip Circumference Hip Circumference Condition rs201770 rs201770 DLEU1

What the study found

Who was studied 186,825 British ancestry men.

The effect Each copy of the G allele shifted the measure 0.0256 lower (95% confidence interval 0.019-0.033); p = 6 × 10−13.

Where it sits Chromosome 13, band 13q14.3 — in an intron of DLEU1.

What each result means

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

Questions about rs201770

What is rs201770?

rs201770 is a single position in the genome, in or near the DLEU1 gene. Published research associates it with hip circumference adjusted for bmi. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs201770 linked to?

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

Does having rs201770 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 rs201770 come from?

GWAS Catalog, Scientific reports 2021, PMID:34021172. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Hip circumference adjusted for BMI (rs201770). MyGeneLog™. https://www.mygenelog.com/variants/rs201770

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