Standard

Body mass index

ASXL3 · rs11081818

Where this position leads

Condition: Obesity and Body Weight

rs11081818 Condition: Obesity and Body Weight Obesity and Body Weight Condition rs11081818 rs11081818 ASXL3

What the study found

Who was studied 315,347 European ancestry individuals, 8,322 Hispanic/Latino individuals, 7,290 East Asian ancestry individuals, 3,069 African American individuals, 459 South Asian ancestry individuals; replicated in 431,743 European ancestry individuals, 9,275 South Asian ancestry individuals, 8,261 African British individuals, 1,822 East Asian ancestry individuals, 7,620 individuals.

The effect Each copy of the A allele shifted the measure 0.014 higher; p = 1 × 10−15.

Where it sits Chromosome 18, band 18q12.1 — in an intron of ASXL3.

What ClinVar records

Classification Benign; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2018-07-26. ClinVar record 1278300 NM_030632.3(ASXL3):c.595+334G>A

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

A/A Two copies of the version the research linked to Body mass index. 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 Body mass index. That is a smaller link than two copies.
G/G No copy of the version the research linked to Body mass index. This is the starting point the study compared everyone against.
Source

Questions about rs11081818

What is rs11081818?

rs11081818 is a single position in the genome, in or near the ASXL3 gene. Published research associates it with body mass index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11081818 linked to?

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

Does having rs11081818 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 rs11081818 come from?

GWAS Catalog, Genetics 2018, PMID:30108127. 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.

Body mass index (rs11081818). MyGeneLog™. https://www.mygenelog.com/variants/rs11081818

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