Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 22, 2026

1,135 positions on this site are linked to Type 2 Diabetes, out of 106,718 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

NF1 · rs2040792

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Sensitive

Type 2 diabetes

UBE3C · rs1002389

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Sensitive

Type 2 diabetes

CYTH1 · rs7224711

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Sensitive

Type 2 diabetes

GNAS-AS1 · rs4810145

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Sensitive

Type 2 diabetes

TET1 · rs10998338

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Sensitive

Type 2 diabetes

XKR6 · rs10086521

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Sensitive

Type 2 diabetes

CT70 · rs4556142

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Sensitive

Type 2 diabetes

HNF4A · rs188520200

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Sensitive

Type 2 diabetes

KCNQ1 · rs4930141

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Sensitive

Type 2 diabetes

ZBTB38 · rs75206890

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Sensitive

Type 2 diabetes

near HNF1B · rs3094503

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Sensitive

Type 2 diabetes

CDC123 · rs11257600

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Sensitive

Type 2 diabetes

PLEKHM2 · rs12746673

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Sensitive

Type 2 diabetes

MSRA · rs60384372

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Sensitive

Type 2 diabetes

VTI1A · rs7100404

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Sensitive

Type 2 diabetes

POU5F1 · rs2844623

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Sensitive

Type 2 diabetes

PCGF3 · rs1531583

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Sensitive

Type 2 diabetes

SLC16A11 · rs13342232

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Sensitive

Type 2 diabetes

near LINC02227 · rs1650505

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Sensitive

Type 2 diabetes

BPTF · rs12603589

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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.