Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,479 positions on this site are linked to Height, out of 2,509,439 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

CFAP206 · rs2179845

See detailed info → Standard

Height

near PCM1 · rs208752

See detailed info → Standard

Height

ABCC8 · rs2074315

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Height

LINC01829 · rs2062203

See detailed info → Standard

Height (baseline)

EZH2 · rs201638335

See detailed info → Standard

Height (baseline)

PPM1B · rs201387534

See detailed info → Standard

Height (baseline)

SLC1A3-AS1 · rs201354674

See detailed info → Standard

Height (standard GWA)

BNC2 · rs1927635

See detailed info → Standard

Height

near APOBEC3AP1 · rs191462864

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Height

TACR3 · rs1905172

See detailed info → Standard

Height

near PRKG2 · rs1901568

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Height

MIR548BAHG · rs1881110

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Height (baseline)

near FGF18 · rs188009752

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Height (baseline)

near IGBP1P3 · rs187378750

See detailed info → Standard

Height (baseline)

near UBE4B · rs186541110

See detailed info → Standard

Height

near SLC5A9 · rs186247912

See detailed info → Standard

Height (baseline)

UHRF1 · rs17885791

See detailed info → Standard

Height (baseline)

CCDC88A · rs17792113

See detailed info → Standard

Height

near CCDC171 · rs17784173

See detailed info → Standard

Height (baseline)

TTLL5 · rs17783174

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Showing 20 of 11479 · page 261 of 574

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.