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 (baseline)

ADAMTSL3 · rs536785166

See detailed info → Standard

Height

LINC01755 · rs4926705

See detailed info → Standard

Height

TWIST1 · rs4721746

See detailed info → Standard

Height (baseline)

MOCS1 · rs41273140

See detailed info → Standard

Height (baseline)

near GNL1 · rs41265836

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Height

near CST5 · rs4074167

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Height

NRXN2-AS1 · rs3825074

See detailed info → Standard

Height (baseline)

CUX1 · rs366345

See detailed info → Standard

Height (standard GWA)

MAP2K1 · rs34842367

See detailed info → Standard

Height

YJU2B · rs346172

See detailed info → Standard

Height (baseline)

LINC00620 · rs34325349

See detailed info → Standard

Height

FAM20C · rs28644307

See detailed info → Standard

Height (standard GWA)

UBE3D · rs2770675

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Height

AHCYL2 · rs2718096

See detailed info → Standard

Height (baseline)

PRKG1 · rs2666543

See detailed info → Standard

Height (standard GWA)

near ARHGAP26 · rs258755

See detailed info → Standard

Height (baseline)

NINJ2 · rs2240893

See detailed info → Standard

Height (baseline)

LINC01755 · rs1963328

See detailed info → Standard

Height (standard GWA)

LINC01621 · rs1960739

See detailed info → Standard

Height

LINC01725 · rs187084421

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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.