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Weight

PLCE1 · rs4918188

Where this position leads

Condition: Obesity and Body Weight

rs4918188 Condition: Obesity and Body Weight Obesity and Body Weight Condition rs4918188 rs4918188 PLCE1

What the study found

Who was studied 507,850 East Asian ancestry individuals, 420,829 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.007 lower (95% confidence interval 0.0045-0.0095); p = 3 × 10−8.

Where it sits Chromosome 10, band 10q23.33 — in an intron of PLCE1.

What ClinVar records

Classification Benign; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2018-11-12. ClinVar record 1264955 NM_016341.4(PLCE1):c.4665+289A>C

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

Questions about rs4918188

What is rs4918188?

rs4918188 is a single position in the genome, in or near the PLCE1 gene. Published research associates it with weight. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs4918188 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 rs4918188 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 rs4918188 come from?

GWAS Catalog, Nature communications 2025, PMID:40436827. 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.

Weight (rs4918188). MyGeneLog™. https://www.mygenelog.com/variants/rs4918188

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