Variants linked to Intelligence

Continuously updated · newest added Sep 16, 2026

303 positions on this site are linked to Intelligence, out of 12,552 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 Intelligence

Standard

Intelligence (MTAG)

EXOC4 · rs4728302

See detailed info →
Standard

Intelligence (MTAG)

RNU1-15P · rs6979354

See detailed info →
Standard

Intelligence (MTAG)

POU6F2-AS2 · rs952623

See detailed info →
Standard

Intelligence (MTAG)

PURG · rs1421334

See detailed info →
Standard

Intelligence (MTAG)

EXOC4 · rs12707116

See detailed info →
Standard

Intelligence (MTAG)

EXOC4 · rs17167210

See detailed info →
Standard

Intelligence (MTAG)

CALN1 · rs2944839

See detailed info →
Standard

Intelligence (MTAG)

RP11-436D23.1 · rs4587178

See detailed info →
Standard

Intelligence (MTAG)

VN1R11P · rs6940638

See detailed info →
Standard

Intelligence (MTAG)

RP11-436D23.1 · rs9401295

See detailed info →
Standard

Intelligence (MTAG)

RP11-436D23.1 · rs1933720

See detailed info →
Standard

Intelligence (MTAG)

RP11-436D23.1 · rs1487439

See detailed info →
Standard

Intelligence (MTAG)

ENSG00000252399 · rs9379850

See detailed info →
Standard

Intelligence (MTAG)

RP11-436D23.1 · rs62422687

See detailed info →
Standard

Intelligence (MTAG)

LACE1 · rs6568547

See detailed info →
Standard

Intelligence (MTAG)

GUSBP2 · rs9379945

See detailed info →
Standard

Intelligence (MTAG)

RP11-436D23.1 · rs1933721

See detailed info →
Standard

Intelligence (MTAG)

GLCCI1 · rs4725065

See detailed info →
Standard

Intelligence (MTAG)

HIST1H1E · rs7749823

See detailed info →
Standard

Intelligence (MTAG)

ENSG00000216915 · rs6940116

See detailed info →

Showing 20 of 303 · page 7 of 16

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.