Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 22, 2026

1,129 positions on this site are linked to Type 2 Diabetes, out of 106,382 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Type 2 Diabetes

Sensitive

Type 2 diabetes

TFAP2B · rs62405419

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Sensitive

Type 2 diabetes

near OR7K1P · rs1955851

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Sensitive

Type 2 diabetes

LINC01524 · rs2426439

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Sensitive

Type 2 diabetes

ROBO2 · rs2272163

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Sensitive

Type 2 diabetes

GIPR · rs61373376

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Sensitive

Type 2 diabetes

INAFM2 · rs3743140

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Sensitive

Type 2 diabetes

LINC00529 · rs2409742

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Sensitive

Type 2 diabetes

near MTDHP3 · rs150182828

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Sensitive

Diabetes

HLA-DQA1 · rs9272364

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Sensitive

Type 2 diabetes

CCND1 · rs3918292

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Sensitive

Type 2 diabetes

KSR2 · rs79310463

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Sensitive

Type 2 diabetes

CTBP1-DT · rs72501962

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Sensitive

Type 2 diabetes

LAMA1 · rs9948462

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Sensitive

Type 2 diabetes

near PPIAP23 · rs9515905

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Sensitive

Type 2 diabetes

near RSPO3 · rs2800733

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Sensitive

Type 2 diabetes

near MACIR · rs75432112

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Sensitive

Type 2 diabetes

HMG20A · rs952472

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Sensitive

Type 2 diabetes

KSR2 · rs7313918

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Sensitive

Type 2 diabetes

CPA1 · rs77792157

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Sensitive

Type 2 diabetes

LIPH · rs147676117

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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.