Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 22, 2026

1,114 positions on this site are linked to Type 2 Diabetes, out of 105,626 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

PLXND1 · rs78252470

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Sensitive

Type 2 diabetes with neurological manifestations (PheCode 250.24)

ZMIZ1 · rs703969

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Sensitive

Type 2 diabetes

ADCY5 · rs60054445

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Sensitive

Type 2 diabetes with ketoacidosis (PheCode 250.21)

near SUMO2P2 · rs550539923

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Sensitive

Type 2 diabetes

near GTF3AP5 · rs17168605

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Sensitive

Type 2 diabetes

GALNT3 · rs13406280

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Sensitive

Type 2 diabetes

PROX1 · rs12403994

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Sensitive

Type 2 diabetes

JARID2 · rs11751816

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Sensitive

Type 2 diabetes

ANK1 · rs117271404

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Sensitive

Type 2 diabetes

LINC02490 · rs75332279

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Sensitive

Type 2 diabetes

NOTCH4 · rs206015

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Sensitive

Type 2 diabetes with ketoacidosis (PheCode 250.21)

PENK-AS1 · rs183360430

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Sensitive

Type 2 diabetes

GRIPAP1 · rs11545861

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Sensitive

Type 2 diabetes

JMJD1C · rs111765639

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Sensitive

Type 2 diabetes

KCNK16 · rs1109772

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Sensitive

Type 2 diabetes

near RNU6-891P · rs6853272

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Sensitive

Type 2 diabetes

IFT52 · rs6073143

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Sensitive

Type 2 diabetes

HNF1B · rs3110649

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Sensitive

Type 2 diabetes

near Y_RNA · rs117526461

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Sensitive

Type 2 diabetes

KDM2B · rs10849893

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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.