Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,129 positions on this site are linked to Height, out of 2,506,525 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

NRXN3 · rs2574750

See detailed info → Standard

Height

near ETV1 · rs41503

See detailed info → Standard

Height

near KCNS3 · rs4404270

See detailed info → Standard

Height

WDR81 · rs62090047

See detailed info → Standard

Height

MECOM · rs62294347

See detailed info → Standard

Height

PDCD6-AHRR · rs62345188

See detailed info → Standard

Height

near SSTR2 · rs6501601

See detailed info → Standard

Height

DDR2 · rs6697469

See detailed info → Standard

Height

MLPH · rs67071074

See detailed info → Standard

Height

near THOC1 · rs694785

See detailed info → Standard

Height

near CLXN · rs6988484

See detailed info → Standard

Height

near CCN6 · rs73537568

See detailed info → Standard

Height

PLCB1 · rs73598282

See detailed info → Standard

Height

ENPP6 · rs78293932

See detailed info → Standard

Height

near CLASP2 · rs79495297

See detailed info → Standard

Height

XXYLT1 · rs952481

See detailed info → Standard

Height

CDKN2C · rs3176468

See detailed info → Standard

Height

DLEU1 · rs75823898

See detailed info → Standard

Height

TARS · rs10071837

See detailed info → Standard

Height

LTBP2 · rs4899520

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Showing 20 of 11129 · page 211 of 557

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.