Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,668 positions on this site are linked to Height, out of 2,512,045 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

ADAMTS17 · rs9672868

See detailed info → Standard

Height

ERC1 · rs7301869

See detailed info → Standard

Height

near LINC02120 · rs17546321

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Height

near HDAC11 · rs2597520

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Height

PPL · rs13335236

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Height

UPF2 · rs10752250

See detailed info → Standard

Height

STK4 · rs6031944

See detailed info → Standard

Height

DLEU1 · rs3118912

See detailed info → Standard

Height

BAG6 · rs10484558

See detailed info → Standard

Height

RABGAP1 · rs10818768

See detailed info → Standard

Height

TESHL · rs10178069

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Height

SLC25A12 · rs6745143

See detailed info → Standard

Height

CTC1 · rs3027247

See detailed info → Standard

Height

CPT1A · rs3019598

See detailed info → Standard

Height

ATF7-NPFF · rs17100298

See detailed info → Standard

Height

XPO7 · rs4872207

See detailed info → Standard

Height

near HIGD1AP18 · rs1545507

See detailed info → Standard

Height

CCDC57 · rs7222764

See detailed info → Standard

Height

MNAT1 · rs1887741

See detailed info → Standard

Height

SMCO3 · rs7963212

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Showing 20 of 11668 · page 48 of 584

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.