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

NFAT5 · rs244415

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Sensitive

Type 2 diabetes

ZZEF1 · rs8068804

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Sensitive

Type 2 diabetes

TEX14 · rs302864

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Sensitive

Type 2 diabetes

TSPAN8 · rs7138300

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Sensitive

Type 2 diabetes

OASL · rs61953351

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Sensitive

Type 2 diabetes

TYRL · rs7929543

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Sensitive

Type 2 diabetes

CHUK · rs11591741

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Sensitive

Type 2 diabetes

ETS1 · rs67232546

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Sensitive

Type 2 diabetes

CTTNBP2 · rs13239186

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Sensitive

Type 2 diabetes

LOC101927450 · rs17791483

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Sensitive

Type 2 diabetes

TP53INP1 · rs7845219

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Sensitive

Type 2 diabetes

UBE3C · rs7786095

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Sensitive

Type 2 diabetes

LOC157273 · rs11774915

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Sensitive

Type 2 diabetes

FAM241B · rs2616132

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Sensitive

Type 2 diabetes

LOC107987099 · rs10114341

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Sensitive

Type 2 diabetes

ST6GAL1 · rs3887925

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Sensitive

Type 2 diabetes

SPATA18 · rs17086692

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Sensitive

Type 2 diabetes

TNIK · rs11925227

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Sensitive

Type 2 diabetes

YTHDC2 · rs10077431

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Sensitive

Type 2 diabetes

LOC105373585 · rs12617659

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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.