Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,560 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 (standard GWA)

near HIVEP2 · rs950932

See detailed info → Standard

Height (baseline)

GLI2 · rs895485

See detailed info → Standard

Height (baseline)

near CASC17 · rs8068231

See detailed info → Standard

Height (baseline)

CCDC91 · rs77342159

See detailed info → Standard

Height

FBXO2 · rs7526268

See detailed info → Standard

Height

GRIN2A · rs7201930

See detailed info → Standard

Height

near C10orf71-AS1 · rs6537521

See detailed info → Standard

Height (baseline)

near POLR1F · rs6461447

See detailed info → Standard

Height (standard GWA)

ZNF423 · rs62029416

See detailed info → Standard

Height

near PTHLH · rs57454081

See detailed info → Standard

Height (baseline)

MAP3K2 · rs55998444

See detailed info → Standard

Height

UIMC1 · rs506370

See detailed info → Standard

Height

near LINC00540 · rs4770263

See detailed info → Standard

Height

ALDH1A3-AS1 · rs4646669

See detailed info → Standard

Height

near SPOCD1 · rs34760089

See detailed info → Standard

Height

ODAD2 · rs2815499

See detailed info → Standard

Height (standard GWA)

LINC02680 · rs2763309

See detailed info → Standard

Height

near RPL21P46 · rs2708987

See detailed info → Standard

Height

PPP6R3 · rs2472429

See detailed info → Standard

Height

DBNL · rs17546439

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Showing 20 of 11491 · page 369 of 575

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.