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 PTEN · rs10887771

See detailed info →
Sensitive

Type 2 diabetes

RASA4 · rs75990271

See detailed info →
Sensitive

Type 2 diabetes

STRBP · rs7026688

See detailed info →
Sensitive

Type 2 diabetes

FAM234A · rs6600208

See detailed info →
Sensitive

Type 2 diabetes

near LINC03042 · rs60128210

See detailed info →
Sensitive

Type 2 diabetes

near HNF4G · rs2920928

See detailed info →
Sensitive

Type 2 diabetes with ketoacidosis (PheCode 250.21)

VGLL3 · rs190767814

See detailed info →
Sensitive

Type 2 diabetes

near RPL13AP22 · rs146295182

See detailed info →
Sensitive

Type 2 diabetes

HIVEP2 · rs11969311

See detailed info →
Sensitive

Diabetic neuropathy in type 2 diabetes

GYPA · rs1132787

See detailed info →
Sensitive

Type 2 diabetes

near LINC02338 · rs9563574

See detailed info →
Sensitive

Type 2 diabetes

SIN3A · rs8038760

See detailed info →
Sensitive

Type 2 diabetes with ophthalmic manifestations (PheCode 250.23)

AUTS2 · rs7801117

See detailed info →
Sensitive

Type 2 diabetes

GRB14 · rs72874860

See detailed info →
Sensitive

Type 2 diabetes

PDIK1L · rs61776586

See detailed info →
Sensitive

Type 2 diabetes

EYA2 · rs6063048

See detailed info →
Sensitive

Type 2 diabetes

KCNQ1 · rs57274815

See detailed info →
Sensitive

Type 2 diabetes

ANKH · rs3845281

See detailed info →
Sensitive

Type 2 diabetes

TMEM18 · rs35913461

See detailed info →
Sensitive

Type 2 diabetes

TM4SF4 · rs34573045

See detailed info →

Showing 20 of 1109 · page 13 of 56

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.