Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,432 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

near FGF6 · rs12580415

See detailed info → Standard

Height (baseline)

AAK1 · rs12476268

See detailed info → Standard

Height

RBM23 · rs1242631

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Height

FCHO2 · rs12189246

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Height

ADAM7-AS1 · rs11991223

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Height

PPIAP78 · rs11955611

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Height

near EEF1B2P6 · rs11769128

See detailed info → Standard

Height (baseline)

LIN28B-AS1 · rs117441937

See detailed info → Standard

Height (baseline)

GOSR1 · rs117431025

See detailed info → Standard

Standing height (UKB data field 50)

TAF4 · rs11699193

See detailed info → Standard

Standing height (UKB data field 50)

near RBM48 · rs116963855

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Height (baseline)

PEAK1 · rs116902949

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Height

PLEKHM3 · rs11679380

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Height

PSMB3 · rs11656344

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Height (baseline)

near RNU5A-2P · rs116139420

See detailed info → Standard

Height

near CDC27 · rs11570441

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Height (baseline)

near OR4A7P · rs11559719

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Height (standard GWA)

MAP3K13 · rs115526731

See detailed info → Standard

Height (baseline)

near LCORL · rs113529840

See detailed info → Standard

Height (baseline)

RUFY4 · rs112940003

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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.