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Waist-to-hip ratio adjusted for BMI

MAPKBP1 · rs890498

What the study found

Who was studied 379,501 European ancestry female individuals.

The effect Each copy of the C allele shifted the measure 0.0151 lower (95% confidence interval 0.011-0.019); p = 3 × 10−15.

How common The C allele had a frequency of about 66% in the people studied.

Where it sits Chromosome 15, band 15q15.1 — in an intron of MAPKBP1.

What ClinVar records

Classification Benign for Malignant lymphoma, large B-cell, diffuse, Uveal melanoma; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2021-05-13. ClinVar record 1182734 NM_014994.3(MAPKBP1):c.2291+143C>G

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 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

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Waist-to-hip ratio adjusted for BMI compared to the general population.
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Waist-to-hip ratio adjusted for BMI.
G/G Published research associates this genotype with typical/baseline likelihood of Waist-to-hip ratio adjusted for BMI — no copies of the reported risk allele.
Source

Questions about rs890498

What is rs890498?

rs890498 is a single position in the genome, in or near the MAPKBP1 gene. Published research associates it with waist-to-hip ratio adjusted for bmi. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs890498 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 rs890498 come from?

GWAS Catalog, Human molecular genetics 2019, PMID:30239722. 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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Waist-to-hip ratio adjusted for BMI (rs890498). MyGeneLog™. https://www.mygenelog.com/variants/rs890498

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