Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 12, 2026

11,879 positions on this site are linked to Height, out of 2,515,960 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 Y_RNA · rs12517663

See detailed info → Standard

Height

near EPHA4 · rs12469320

See detailed info → Standard

Height

CARS1 · rs12363575

See detailed info → Standard

Height (baseline)

CARNS1 · rs12288107

See detailed info → Standard

Height

IFI16 · rs12239437

See detailed info → Standard

Height

LNC-LBCS · rs12199312

See detailed info → Standard

Height

near HLA-DOA · rs12190787

See detailed info → Standard

Height (baseline)

near RNU6-543P · rs12146192

See detailed info → Standard

Height (standard GWA)

ECRG4 · rs11903518

See detailed info → Standard

Height

DYSF · rs11894210

See detailed info → Standard

Height

PLEC1 · rs11783655

See detailed info → Standard

Height (baseline)

AFG1L · rs117638195

See detailed info → Standard

Height (baseline)

ADAMTSL3 · rs117427668

See detailed info → Standard

Height

WWC2 · rs11730648

See detailed info → Standard

Height (baseline)

HDAC9 · rs116904069

See detailed info → Standard

Height (baseline)

near SPINK2 · rs116769300

See detailed info → Standard

Height (baseline)

near KLF11 · rs11674455

See detailed info → Standard

Height (baseline)

near Y_RNA · rs116499608

See detailed info → Standard

Height (baseline)

near SOD1P2 · rs11648575

See detailed info → Standard

Height

CNOT1 · rs11644694

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Showing 20 of 11879 · page 353 of 594

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.