Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,507 positions on this site are linked to Height, out of 2,509,834 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

ZNF710 · rs2970357

See detailed info → Standard

Height

RREB1 · rs7743323

See detailed info → Standard

height (minimum, inv-normal transformed)

RAB3GAP1 · rs115227414

See detailed info → Standard

height (mean, inv-normal transformed)

MTOR · rs1148480

See detailed info → Standard

Height

near ZFP36L1 · rs7146217

See detailed info → Standard

Height

DISP1 · rs139405583

See detailed info → Standard

Height

MYO9B · rs2305769

See detailed info → Standard

Height

CCDC26 · rs4636162

See detailed info → Standard

Height

PARP1 · rs932002

See detailed info → Standard

Height

FGL1 · rs10099622

See detailed info → Standard

Height

near CDYL · rs13204938

See detailed info → Standard

Height

SLC16A12 · rs1331147

See detailed info → Standard

Height

DOCK4 · rs149092986

See detailed info → Standard

Height

near RNF122 · rs149683285

See detailed info → Standard

Height

near ZNF706 · rs149823188

See detailed info → Standard

Height

LMOD3 · rs150646386

See detailed info → Standard

Height

ADGRB3 · rs150728431

See detailed info → Standard

Height

near ZNF385B · rs151230422

See detailed info → Standard

Height

near CHL1 · rs17325178

See detailed info → Standard

Height

ZNF704 · rs17474841

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Showing 20 of 11507 · page 567 of 576

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.