Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,639 positions on this site are linked to Height, out of 2,511,480 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

KLHL29 · rs1991083

See detailed info → Standard

Height

CABLES1 · rs17186875

See detailed info → Standard

Height

CRADD · rs1471816

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Height

near C17orf67 · rs1401796

See detailed info → Standard

Height

IGF1R · rs13379905

See detailed info → Standard

Height

near KRT18P35 · rs13072100

See detailed info → Standard

Height

DLEU1 · rs1262774

See detailed info → Standard

Height

HAGHL · rs12448432

See detailed info → Standard

Height

near PTCH1 · rs12343296

See detailed info → Standard

Height

near ZMIZ1 · rs11002928

See detailed info → Standard

Height

CDC14B · rs10991378

See detailed info → Standard

Height

near AK4P2 · rs10940473

See detailed info → Standard

Height

GFPT2 · rs1035412

See detailed info → Standard

Height

ITGB8 · rs10265149

See detailed info → Standard

Height

DIS3L2 · rs76803230

See detailed info → 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

See detailed info → Standard

Height

QSOX2 · rs12338076

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Showing 20 of 11639 · page 13 of 582

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.