Standard

Hip circumference adjusted for BMI

ZNF341 · rs4911132

Where this position leads

Condition: Hip Circumference

rs4911132 Condition: Hip Circumference Hip Circumference Condition rs4911132 rs4911132 ZNF341

What the study found

Who was studied 219,872 British ancestry women.

The effect Each copy of the G allele shifted the measure 0.0213 lower (95% confidence interval 0.015-0.027); p = 6 × 10−13.

Where it sits Chromosome 20, band 20q11.22 — in an intron of ZNF341.

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 rs4911132

What is rs4911132?

rs4911132 is a single position in the genome, in or near the ZNF341 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 rs4911132 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 rs4911132 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 rs4911132 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 (rs4911132). MyGeneLog™. https://www.mygenelog.com/variants/rs4911132

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