Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,452 positions on this site are linked to Height, out of 2,509,249 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 (baseline)

SCAF4 · rs7280330

See detailed info → Standard

Height (baseline)

WWP2 · rs72785073

See detailed info → Standard

Height (standard GWA)

near GPIHBP1 · rs72691642

See detailed info → Standard

Height

CHD9NB · rs7194847

See detailed info → Standard

Height

CSGALNACT1 · rs6983139

See detailed info → Standard

Height (baseline)

LINC02463 · rs697881

See detailed info → Standard

Height (baseline)

near CEP120 · rs6881525

See detailed info → Standard

Height (baseline)

DENND6A · rs6790873

See detailed info → Standard

Height

PATJ · rs6688017

See detailed info → Standard

Height (baseline)

PROX2 · rs66591704

See detailed info → Standard

Height (baseline)

PPM1E · rs6503882

See detailed info → Standard

Height

near RPL7P37 · rs644556

See detailed info → Standard

Height (baseline)

DPY19L1P2 · rs62465331

See detailed info → Standard

Height (baseline)

near RNA5SP228 · rs62448660

See detailed info → Standard

Height (baseline)

near LINC01991 · rs62278038

See detailed info → Standard

Height (baseline)

LINC01267 · rs62231804

See detailed info → Standard

Height (baseline)

RBMS1 · rs62175966

See detailed info → Standard

Height (baseline)

near UBE2Q2P2 · rs62011082

See detailed info → Standard

Height (standard GWA)

E2F7 · rs61932773

See detailed info → Standard

Height (baseline)

PCSK2 · rs6080699

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Showing 20 of 11452 · page 246 of 573

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.