Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 6, 2026

1,535 positions on this site are linked to Height, out of 2,500,639 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

TRIB1AL · rs2954025

See detailed info → Standard

Height

NFKB1-AS1 · rs980455

See detailed info → Standard

Height (baseline)

EIF2AK3 · rs7593335

See detailed info → Standard

Height

near SKI · rs2460000

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Height

QSOX2 · rs12338076

See detailed info → Standard

Height

LPP · rs4686991

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Height

THOC1 · rs8087639

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Height

near HLA-DQA1 · rs9271348

See detailed info → Standard

Height

ITGB8 · rs1023522

See detailed info → Standard

Height

SMAD6 · rs7179372

See detailed info → Standard

Height

LRRC69 · rs4339600

See detailed info → Standard

Height

SENP2 · rs3087964

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height (mean, inv-normal transformed)

near TBX2-AS1 · rs11868532

See detailed info → Standard

Height

DOT1L · rs12982744

See detailed info → Standard

Height

near PSCA · rs2976397

See detailed info → Standard

Height

near NHEJ1 · rs359974

See detailed info → Standard

Height

HSPG2 · rs9426785

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Height

CCND2 · rs3217844

See detailed info → Standard

Height

PVT1 · rs4733789

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

LCORL · rs6842114

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Showing 20 of 1535 · page 1 of 77

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.