Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,645 positions on this site are linked to Height, out of 2,511,711 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

NPAS3 · rs1956002

See detailed info → Standard

Height

BMP6 · rs9505293

See detailed info → Standard

Height

near AK3P4 · rs2900095

See detailed info → Standard

Height

ELAVL1 · rs12972375

See detailed info → Standard

Height

near FKBP7 · rs2288323

See detailed info → Standard

Height

LINC01752 · rs2144184

See detailed info → Standard

Height

SLC2A1 · rs16830101

See detailed info → Standard

Height

TULP3 · rs7303345

See detailed info → Standard

Height

DHRS4-AS1 · rs7146599

See detailed info → Standard

Height

BRD1 · rs138841

See detailed info → Standard

Height

EXTL3 · rs9183

See detailed info → Standard

Height

NCOR2 · rs837491

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Height

near LCORL · rs10488993

See detailed info → Standard

Height

FAIM · rs361074

See detailed info → Standard

Height

RPS9 · rs17239559

See detailed info → Standard

Height

HMGA2 · rs1460126

See detailed info → Standard

Height

ANKRD27 · rs8100423

See detailed info → Standard

Height

ADGRV1 · rs7707023

See detailed info → Standard

Height

LUM · rs3168534

See detailed info → Standard

Height

EIF2AK3 · rs6739095

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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.