Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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

CREB3L1 · rs2303435

See detailed info → Standard

Height

RDM1 · rs2280786

See detailed info → Standard

Height

NCSTN · rs2274185

See detailed info → Standard

Height (baseline)

NMT1 · rs2239924

See detailed info → Standard

Height

MEF2C-AS1 · rs2217257

See detailed info → Standard

Height

LINC02834 · rs2026343

See detailed info → Standard

Height

LINC02822 · rs2014116

See detailed info → Standard

Standing height (UKB data field 50)

LINC00092 · rs192497183

See detailed info → Standard

Height

near TTC4P1 · rs1917773

See detailed info → Standard

Height (baseline)

near CCR4 · rs187911095

See detailed info → Standard

Height (baseline)

UBXN2A · rs186538776

See detailed info → Standard

Height (baseline)

near TXNRD1 · rs186033146

See detailed info → Standard

Height

AKAP1 · rs17833741

See detailed info → Standard

Height

near BHLHE40 · rs17789885

See detailed info → Standard

Height (baseline)

CBLIF · rs17596862

See detailed info → Standard

Height (baseline)

ZNF346 · rs17572473

See detailed info → Standard

Height

IGFALS · rs17559

See detailed info → Standard

Height

SGCZ · rs17471747

See detailed info → Standard

Height (baseline)

COL24A1 · rs17402103

See detailed info → Standard

Height

SPSB1 · rs17377604

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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.