Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 22, 2026

1,109 positions on this site are linked to Type 2 Diabetes, out of 105,248 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

near OR5B17 · rs7483027

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Sensitive

Type 2 diabetes

near BMPR2 · rs6714523

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Sensitive

Type 2 diabetes

near TM4SF4 · rs28712435

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Sensitive

Type 2 diabetes

TCF7L2 · rs193023456

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Sensitive

Type 2 diabetes

TLE4 · rs1328412

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Sensitive

Type 2 diabetes

MDM4 · rs12039968

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Sensitive

Type 2 diabetes

near CRYBA1 · rs9913225

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Sensitive

Type 2 diabetes

MYEOV · rs28599796

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Sensitive

Type 2 diabetes

LMF1 · rs12918782

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Sensitive

Type 2 diabetes

THRAP3 · rs11576244

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Sensitive

Body fat percentage and type 2 diabetes (pairwise)

CENPW · rs9385400

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Sensitive

Type 2 diabetes

CPEB3 · rs7920520

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Sensitive

Type 2 diabetes with neurological manifestations (PheCode 250.24)

NOTCH2 · rs72697237

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Sensitive

Type 2 diabetes

near EIF4E2P2 · rs6438247

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Sensitive

Type 2 diabetes

OSER1 · rs6073369

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Sensitive

Type 2 diabetes with ketoacidosis (PheCode 250.21)

near LINC02353 · rs565381963

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Sensitive

Type 2 diabetes

near ZNF257 · rs4932747

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Sensitive

Type 2 diabetes

near PPIAP9 · rs2534653

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Sensitive

Type 2 diabetes

PKIG · rs244080

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Sensitive

Type 2 diabetes with ketoacidosis (PheCode 250.21)

near NUP50P4 · rs138922162

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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.