Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,015 positions on this site are linked to Height, out of 2,506,010 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 ALX4 · rs2863089

See detailed info → Standard

Height

LSM4 · rs2232965

See detailed info → Standard

Standing height (UKB data field 50)

LINC02456 · rs187099365

See detailed info → Standard

Height

ZFAT · rs17700513

See detailed info → Standard

Height

SLC16A1-AS1 · rs17030905

See detailed info → Standard

Height

PRKCA · rs9901804

See detailed info → Standard

Height

PPP2R2D · rs7085239

See detailed info → Standard

Height

ZNF638 · rs6740645

See detailed info → Standard

Height

VCPIP1 · rs3824258

See detailed info → Standard

Height

NEDD4 · rs17819282

See detailed info → Standard

Height

SLC1A7 · rs1769309

See detailed info → Standard

Height

CCDC26 · rs16904148

See detailed info → Standard

Height

near MECOM · rs16853096

See detailed info → Standard

Height

near RPL24P7 · rs12638485

See detailed info → Standard

Height (baseline)

near HLA-DQB1 · rs9274922

See detailed info → Standard

Height

LY86-AS1 · rs7767578

See detailed info → Standard

Height

CUX2 · rs6490029

See detailed info → Standard

Height

FBXW11 · rs17682767

See detailed info → Standard

Height

LBH · rs17322097

See detailed info → Standard

Height

UBR1 · rs16957385

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Showing 20 of 11015 · page 167 of 551

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.