Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 22, 2026

1,132 positions on this site are linked to Type 2 Diabetes, out of 106,592 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

AGPAT9 · rs201597274

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Sensitive

Type 2 diabetes

MAML3 · rs12505942

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Sensitive

Type 2 diabetes

NYNRIN · rs12437434

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Sensitive

Type 2 diabetes

LINC02450 · rs11181613

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Sensitive

Type 2 diabetes

BMAL1 · rs7949336

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Sensitive

Type 2 diabetes

PPARG · rs709156

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Sensitive

Type 2 diabetes

STEAP2-AS1 · rs6978118

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Sensitive

Type 2 diabetes

DTNB · rs34845373

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Sensitive

Type 2 diabetes

near PARP8 · rs152839

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Sensitive

Type 2 diabetes

HDAC9 · rs583769

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Sensitive

Type 2 diabetes

LINC01991 · rs2292893

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Sensitive

Type 2 diabetes

SLC43A2 · rs9893867

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Sensitive

Type 2 diabetes

CPQ · rs149364428

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Sensitive

Type 2 diabetes

HSD17B12 · rs1061810

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Sensitive

Type 2 diabetes

near C20orf181 · rs4809369

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Sensitive

Type 2 diabetes

ASCC2 · rs36575

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Sensitive

Type 2 diabetes

FAF1-AS1 · rs1278516

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Sensitive

Type 2 diabetes

near MFSD4BP1 · rs12187734

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Sensitive

Type 2 diabetes

SHOC2 · rs7895872

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Sensitive

Type 2 diabetes

INSR · rs75253922

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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.