Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,659 positions on this site are linked to Height, out of 2,511,952 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

near RPSAP49 · rs17054025

See detailed info → Standard

Height

LINC02895 · rs867043

See detailed info → Standard

Height

near SLC39A11 · rs7216472

See detailed info → Standard

Height (baseline)

TSBP1-AS1 · rs2894250

See detailed info → Standard

Height

MTA3 · rs13028484

See detailed info → Standard

Height

KPNA3 · rs17073314

See detailed info → Standard

Height

near SRSF3P1 · rs4757695

See detailed info → Standard

Height

DYM · rs895670

See detailed info → Standard

Height

ARID1A · rs35617712

See detailed info → Standard

Height

ARHGAP26 · rs2578602

See detailed info → Standard

Height

ADAMTS6 · rs11746271

See detailed info → Standard

Height

DPP3 · rs4930379

See detailed info → Standard

Height

IGFBP7 · rs11573106

See detailed info → Standard

Height

near RNU6-63P · rs9579096

See detailed info → Standard

Height (baseline)

DLEU2 · rs2740544

See detailed info → Standard

Height

near SLC38A4-AS1 · rs7975211

See detailed info → Standard

Height

CERS3-AS1 · rs7181754

See detailed info → Standard

Height

RGS3 · rs7021491

See detailed info → Standard

Height

PLPPR1 · rs4278208

See detailed info → Standard

Height

COLGALT2 · rs2378790

See detailed info →

Showing 20 of 11659 · page 44 of 583

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.