Variants linked to Type 2 Diabetes

Continuously updated · newest added Oct 21, 2026

1,098 positions on this site are linked to Type 2 Diabetes, out of 104,576 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

TLE4 · rs17791513

See detailed info →
Standard

Glycated hemoglobin levels

G6PC2 · rs3755157

See detailed info →
Standard

Glycated hemoglobin levels

MYO9B · rs11667918

See detailed info →
Standard

Glycated hemoglobin levels

FN3K · rs1046875

See detailed info →
Sensitive

Type 2 diabetes

FAF1 · rs17106184

See detailed info →
Sensitive

Type 2 diabetes

TMEM154 · rs6813195

See detailed info →
Sensitive

Type 2 diabetes

GLIS3 · rs10814916

See detailed info →
Sensitive

Type 2 diabetes

FAM58A · rs12010175

See detailed info →
Sensitive

Type 2 diabetes

GRK5 · rs10886471

See detailed info →
Standard

Glycated hemoglobin levels

ATP11A · rs7998202

See detailed info →
Sensitive

Type 2 diabetes

CDKN2A · rs10965250

See detailed info →
Sensitive

Type 2 diabetes

JAZF1 · rs849134

See detailed info →
Sensitive

Type 2 diabetes

C6orf57 · rs1048886

See detailed info →
Sensitive

Type 2 diabetes

HNF4A · rs4812829

See detailed info →
Standard

Glycated hemoglobin levels

ANK1 · rs6474359

See detailed info →
Sensitive

Type 2 diabetes

IGF2BP2 · rs1470579

See detailed info →
Sensitive

Type 2 diabetes

HNF1A · rs7957197

See detailed info →
Sensitive

Type 2 diabetes

KCNQ1 · rs231362

See detailed info →
Sensitive

Type 2 diabetes

SLC30A8 · rs3802177

See detailed info →
Sensitive

Type 2 diabetes

KCNJ11 · rs5215

See detailed info →

Showing 20 of 1098 · page 54 of 55

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.