Gene Knowledge Graph
UTC

Variants linked to Waist Circumference

Continuously updated · newest added Sep 13, 2026

58 positions on this site are linked to Waist Circumference, out of 7,670 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Standard

BMI (adjusted for smoking behaviour)

EPHA3 · rs2173039

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BMI (adjusted for smoking behaviour)

INADL · rs2481665

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Waist-to-hip ratio adjusted for BMI (adjusted for smoking behaviour)

MAP3K1 · rs30000

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Body mass index (joint analysis main effects and smoking interaction)

CADM2 · rs13078960

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Body mass index (joint analysis main effects and smoking interaction)

CCDC39 · rs13069244

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Body mass index (joint analysis main effects and smoking interaction)

C6orf106 · rs205262

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Body mass index (joint analysis main effects and smoking interaction)

CCDC95 · rs4787491

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Waist circumference adjusted for BMI in active individuals

SPAG17 · rs7513580

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Waist circumference adjusted for BMI in active individuals

PBRM1 · rs13083798

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Waist circumference adjusted for BMI in active individuals

RSPO3 · rs1936807

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Waist circumference adjusted for BMI in active individuals

ADAMTS9 · rs7638389

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Waist circumference adjusted for BMI in active individuals

DNM3 · rs1894633

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Waist circumference adjusted for BMI in active individuals

DNMT3A · rs11694842

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Waist circumference adjusted for body mass index

ZSCAN2 · rs7176527

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Waist circumference adjusted for body mass index

NSD1 · rs3088050

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Waist circumference adjusted for body mass index

ITGB8 · rs10231365

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Waist circumference adjusted for body mass index

CCDC91 · rs10843151

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Waist circumference adjusted for body mass index

NUCB2 · rs2051773

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Waist circumference adjusted for body mass index

VPS53 · rs741677

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Waist circumference adjusted for body mass index

MEF2C · rs6892330

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.