Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,970 positions on this site are linked to Height, out of 114,540 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 Height

Standard

Height

PLEC1 · rs11783655

See detailed info →
Standard

Height (baseline)

AFG1L · rs117638195

See detailed info →
Standard

Height (baseline)

ADAMTSL3 · rs117427668

See detailed info →
Standard

Height

WWC2 · rs11730648

See detailed info →
Standard

Height (baseline)

HDAC9 · rs116904069

See detailed info →
Standard

Height (baseline)

near SPINK2 · rs116769300

See detailed info →
Standard

Height (baseline)

near KLF11 · rs11674455

See detailed info →
Standard

Height (baseline)

near Y_RNA · rs116499608

See detailed info →
Standard

Height (baseline)

near SOD1P2 · rs11648575

See detailed info →
Standard

Height

CNOT1 · rs11644694

See detailed info →
Standard

Height (baseline)

KIF9 · rs116252905

See detailed info →
Standard

Height (baseline)

near LINC02547 · rs11605159

See detailed info →
Standard

Height (standard GWA)

TOMM20 · rs11582001

See detailed info →
Standard

Height (baseline)

FAM184B · rs115398829

See detailed info →
Standard

Height (baseline)

NELFE · rs114969413

See detailed info →
Standard

Height (baseline)

near CMPK1P1 · rs114466461

See detailed info →
Standard

Height (baseline)

GBF1 · rs113676575

See detailed info →
Standard

Height (baseline)

PPP1R13B · rs113419453

See detailed info →
Standard

Height

SLCO2B1 · rs11236368

See detailed info →
Standard

Height (baseline)

near TRIM51CP · rs111648199

See detailed info →

Showing 20 of 9970 · page 79 of 499

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.