Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,048 positions on this site are linked to Height, out of 2,506,152 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

CENPO · rs1550115

See detailed info → Standard

Height

near EFEMP1 · rs11680015

See detailed info → Standard

Height (baseline)

LTBP1 · rs115016986

See detailed info → Standard

Height (baseline)

SPC25 · rs12993143

See detailed info → Standard

Height (baseline)

EPB41L1 · rs78744669

See detailed info → Standard

Height

ZNF76 · rs6934083

See detailed info → Standard

Standing height (UKB data field 50)

LINC-PINT · rs62473545

See detailed info → Standard

Height

EPAS1 · rs4952818

See detailed info → Standard

Height

AL354740.1 · rs2780215

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

near KCNS3 · rs16984932

See detailed info → Standard

Height

GRM4 · rs79658451

See detailed info → Standard

Height (baseline)

NF1 · rs148378911

See detailed info → Standard

Height

ADAMTSL3 · rs2401171

See detailed info → Standard

Height (baseline)

near TRCG1P · rs1565496

See detailed info → Standard

Height (baseline)

ADAMTSL3 · rs117138192

See detailed info → Standard

Height (baseline)

near IGF1 · rs855206

See detailed info → Standard

Standing height (UKB data field 50)

KCTD5 · rs77844870

See detailed info → Standard

Height

CYCSP55 · rs6913361

See detailed info → Standard

Standing height (UKB data field 50)

RAVER2 · rs34365651

See detailed info → Standard

Height (baseline)

near NCOA1 · rs186490656

See detailed info →

Showing 20 of 11048 · page 177 of 553

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.