Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 22, 2026

1,113 positions on this site are linked to Type 2 Diabetes, out of 105,416 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

PITPNC1 · rs77746881

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Sensitive

Type 2 diabetes

near BPTF · rs3936134

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Sensitive

Type 2 diabetes

near KPNA2 · rs8076753

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Sensitive

Type 2 diabetes

near GRP · rs9957320

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Sensitive

Type 2 diabetes

near MC4R · rs1379443

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Sensitive

Type 2 diabetes

L3MBTL2 · rs139478

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Sensitive

Type 2 diabetes (age of onset)

CDKAL1 · rs9368219

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Sensitive

Type 2 diabetes (age of onset)

near WDR11 · rs3011366

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Sensitive

Type 2 diabetes

near PDZRN3 · rs188048049

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Sensitive

High triglyceride trajectory in type 2 diabetes

APOC3 · rs2854116

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Sensitive

High triglyceride trajectory in type 2 diabetes

near BUD13 · rs61346349

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Sensitive

High triglyceride trajectory in type 2 diabetes

near BUD13 · rs75662937

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Sensitive

Type 2 diabetes

PAX4 · rs2233580

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Sensitive

Type 2 diabetes

CEP68 · rs7572857

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Sensitive

Type 2 diabetes

CENTD2 · rs56200889

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Sensitive

Type 2 diabetes

PCSK6 · rs6598475

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Sensitive

Childhood onset type 2 diabetes

MC4R · rs72982988

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Sensitive

Childhood onset type 2 diabetes

PHF2 · rs10992863

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Sensitive

Childhood onset type 2 diabetes

SLC16A11 · rs113748381

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Sensitive

Severe diabetic retinopathy in type 2 diabetes

NOX4 · rs11018670

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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.