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)

ELAVL2 · rs2026037

See detailed info →
Standard

Intelligence (MTAG)

HPS6 · rs11191205

See detailed info →
Standard

Intelligence (MTAG)

SORCS3 · rs1947988

See detailed info →
Standard

Intelligence (MTAG)

RUNX1T1 · rs2916247

See detailed info →
Standard

Intelligence (MTAG)

C10orf76 · rs117883100

See detailed info →
Standard

Intelligence (MTAG)

JMJD1C · rs6479901

See detailed info →
Standard

Intelligence (MTAG)

C10orf76 · rs67497633

See detailed info →
Standard

Intelligence (MTAG)

RALYL · rs117893056

See detailed info →
Standard

Intelligence (MTAG)

FGF8 · rs7077446

See detailed info →
Standard

Intelligence (MTAG)

CDC14B · rs6477493

See detailed info →
Standard

Intelligence (MTAG)

LRRC14 · rs2721173

See detailed info →
Standard

Intelligence (MTAG)

ENSG00000201074 · rs13287066

See detailed info →
Standard

Intelligence (MTAG)

PHF2 · rs10992797

See detailed info →
Standard

Intelligence (MTAG)

NCOA2 · rs57994514

See detailed info →
Standard

Intelligence (MTAG)

ENSG00000253143 · rs1481045

See detailed info →
Standard

Intelligence (MTAG)

ZMIZ2 · rs3735478

See detailed info →
Standard

Intelligence (MTAG)

EXOC4 · rs17167210

See detailed info →
Standard

Intelligence (MTAG)

ENSG00000241204 · rs13259522

See detailed info →
Standard

Intelligence (MTAG)

EXOC4 · rs12707116

See detailed info →
Standard

Intelligence (MTAG)

PDE1C · rs9648380

See detailed info →

Showing 20 of 303 · page 6 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.